Pesticidal carboxamides

ABSTRACT

The object of the present invention is to provide novel carboxamides which exhibit an excellent pesticidal activity as pesticides. Disclosed are the carboxamides represented by the following Formula (I): 
                         
wherein each substituent is as defined in the specification, and use thereof as pesticides and animal parasite controlling agents.

This application is a 371 of PCT/EP2010/004739, filed Aug. 3, 2010.

TECHNICAL FIELD

The present invention relates to pesticidal carboxamides and their use as pesticides.

BACKGROUND ART

Pesticidal carboxamide compounds are useful as agents for controlling harmful organisms.

EP 1 661 886 A1 (WO 2005/021488), EP 1 714 958 A1 (WO 2005/073165), EP 1 916 236 A1 (WO 2006/137395), EP 1 911 7510 A1 (WO 2006/137376), WO 2008/000438, WO 2008/012027, WO 2008/031534, WO 2008/074427, WO 2008/107091, WO 2009/049844, WO 2009/049845, WO 2007/017075, JP 2006/306771, JP2007/302617 and JP 2007/099761 A refer to insecticidal compounds. WO 2007/128410, WO 2007/051560 discloses insecticidal compounds having a 5 membered ring-system in the core structure.

SUMMARY OF THE INVENTION

Inventors of the present invention extensively studied to develop novel compounds which are highly active as pesticides and have a broad spectrum use. As a result, the inventors found that the novel carboxamides represented by the following Formula (I) have a high activity, a broad spectrum use and safety, and also are effective against harmful pests that are resistant to organic phosphorous agents or carbamate agents.

wherein

-   A¹, A², A³, A⁴ and A⁵ each independently represent nitrogen, C—X¹ or     C-T, provided that at least one of A¹, A², A³, A⁴ and A⁵ is C-T; -   B¹, B², B³, B⁴ and B⁵ each independently represent nitrogen, C—X² or     C-J, provided that at least one of B′, B², B³, B⁴ and B⁵ is C-J; -   G represents oxygen or sulfur; -   Q represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, (C₁₋₁₂     alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₁₋₁₂ alkoxy)carbonyl or     (C₁₋₁₂ haloalkoxy)carbonyl; -   X¹ and X² each independently represent hydrogen, cyano, halogen,     nitro, hydroxy, mercapto, amino, formyl, oxide, C₁₋₁₂ alkyl, C₁₋₁₂     haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂     alkyl-O—, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂     alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂     haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂     haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(═O)₂O—, aryl-O—, aryl-NH—,     aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—,     heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—,     heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂     alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂     alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂     alkyl-S(O)₂—C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂     haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂     haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂     haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl,     aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl,     aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl,     aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl,     heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl,     heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl,     heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈     cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈     halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl,     C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂     haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl,     C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂     alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂     alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂     haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂     haloalkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl,     C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂     haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂     haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbony, (C₃₋₈     halocycloalkoxy)carbony, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbony, C₃₋₈     halocycloalkyl-(C₁₋₁₂ alkoxy)carbony, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂     haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈     halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl,     (C₃₋₈ halocycloalkyl)-(C₁₋₁₂)alkyl-carbonyl, an aryl group, a     heterocyclic group, sulfur pentafluoride, or one of the substituents     represented by the following Formulae (X1-1) to (X1-5):

wherein G independently has the same meaning as G described above;

X³, X⁴ and X⁵ each independently represent hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂ alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂ haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbony, (C₃₋₈ halocycloalkoxy)carbony, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbony, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbony, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₄₂)alkyl-carbonyl, aryl-carbonyl, heterocyclyl-carbonyl, aryl-(C₁₋₁₂)alkyl-carbonyl, heterocyclyl-(C₁₋₁₂)alkyl-carbonyl, sulfur pentafluoride, an aryl group or a heterocyclic group,

X³ and X⁴ may form a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded,

X³ and X⁵ may form a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded;

X⁶ each independently represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, C₃₋₈ cycloalkyl, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, an aryl group, a heterocyclic group, aryl-(C₁₋₁₂)alkyl or heterocyclyl-(C₁₋₁₂)alkyl;

X⁷ each independently represents hydrogen, nitro, cyano, formyl, X⁸-carbonyl or X⁸-oxycarbonyl,

wherein X⁸ independently has the same meaning as X⁶ described above;

J each independently represents C₁₋₁₂ haloalkyl, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(═O)—, C₁₋₁₂ haloalkyl-S(═O)₂—, C₃₋₈ halocycloalkyl, —C(J¹)(J²)(J³) or —C (J¹)(J²)(OJ⁴),

wherein J¹ and J² each independently represent C₁₋₁₂ haloalkyl,

J³ represents a heterocyclic group,

J⁴ represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, C₁₋₁₂ alkylsulfonyl, C₁₋₁₂ haloalkylsulfonyl, arylsulfonyl, an aryl group or a heterocyclic group;

T represents a 5- to 6-membered heterocycle or any one of the substituents represented by the following Formulae (X2-1) to (X2-4):

wherein

X³, X⁵ and G independently have the same meaning as X³, X⁵ and G defined above, respectively;

X⁹, X¹⁰ and X¹¹ each independently have the same meaning as X³, X⁴ and X⁵ defined above, respectively,

X⁹ and X¹⁰ may form a 3- to 8-membered carbon ring or heterocycle, together with the carbon atom to which they are bonded,

X⁹ and X⁵, X¹⁰ and X⁵, or X¹¹ and X⁵ may together form C₁₋₄ alkylene;

R12 and R13 have the same meaning as X⁹ and X¹⁰, respectively,

R14 has the same meaning as X³ described above, and

R15 represents hydrogen;

-   when A¹, A², A³, A⁴ or A⁵ is C-T and T represents any one of the     substituents represented by Formulae (X2-1) to (X2-4), then X⁹, X¹⁰,     X¹¹ or X³ in T may form C₁₋₄ alkylene together with X¹ if A¹, A²,     A³, A⁴ or A⁵ that is adjacent to the carbon atom to which T in C-T     is bonded is C—X¹, and one —CH₂— at any position in the alkylene may     be replaced by —O—, —S— or —NH—; -   when both A¹ and A² represent C—X¹ then X¹'s in the C—X¹'s may form     a 5- to 6-membered saturated or unsaturated carbon ring or     heterocycle, together with the carbon atoms to which X¹'s in C—X¹'s     are bonded, and when both A³ and A⁴ represent C—X¹, then X¹'s in the     C—X¹'s may form a 5- to 6-membered saturated or unsaturated carbon     ring or heterocycle, together with the carbon atoms to which X¹'s in     C—X¹'s are bonded; -   m each independently represents an integer of 1 to 4; and -   each substituent defined above may be further substituted with any     substituent.

The compounds of Formula (I) of the present invention can be obtained according to the following Preparation method (a) to (g), for example.

Preparation Method (a)

A method comprising reacting the compounds represented by Formula (II):

(wherein A¹, A², A³, A⁴, A⁵ and G are as defined above, and L¹ represents hydroxy or an appropriate leaving group, for example chlorine, bromine, a C₁₋₄ alkyl-carbonyloxy group, a C₁₋₄ alkoxy-carbonyloxy group, an azolyl group, a C₁₋₄ alkylsulfonyloxy group, a C₁₋₄ haloalkylsulfonyloxy group, or an arylsulfonyloxy group)

-   with the compounds represented by Formula (III):

(wherein B¹ to B⁵ and Q are as defined above) in the presence of a condensing agent, a base or an appropriate diluent, if necessary.

Preparation Method (b) (when at Least one of A¹, A², A³, A⁴ and A⁵ in Formula (I) is any one of C-W1 to C-W9 as Defined herein (see, paragraph [0035])

A method comprising reacting the compounds represented by Formula (IV):

(wherein B¹ to B⁵, G and Q are as defined above, and A¹⁻¹, A¹⁻², A¹⁻³, A¹⁻⁴ and A¹⁻⁵ independently have the same meaning as A¹ to A⁵ defined above, respectively, with the proviso that at least one of A¹⁻², A¹⁻³, A¹⁻⁴ and A¹⁻⁵ is C-halogen)

-   with the compounds represented by W1-H, W2-H, W3-H, W4-H, W5-H,     W6-H, W7-H, W8-H or W9-H (wherein W1 to W9 are as defined below) in     the presence of an appropriate base, a catalyst or a diluent, if     necessary.

Preparation Method (c) [when at Least One of A¹, A², A³, A⁴ and A⁵ in Formula (I) is C—(X2-1) or C—(X2-2) Having the Same Meaning as Defined Above]

A method comprising reacting the compounds represented by Formula (I-c1):

[wherein B¹ to B⁵, G and Q are as defined above, and A²⁻¹, A²⁻², A²⁻³, A²⁻⁴ and A²⁻⁵ independently have the same meaning as A¹ to A⁵ defined above, respectively, with the proviso that at least one of A²⁻¹, A²⁻², A²⁻³, A²⁻⁴ and A²⁻⁵ is Formula (X3-1):

and X⁹, X¹⁰ and m are as defined above]

-   with the compounds represented by Formula (r-1-1):

(wherein X⁵ and L¹ are as defined above), or

-   with the compounds represented by Formula (r-1-2):

(wherein X⁵ and L¹ are as defined above) or

-   with acid anhydrides of the respective compounds in the presence of     an appropriate base, a condensing agent or a diluent, if necessary,     and -   further, with the compounds represented by Formula (r-2):     X³-L¹  (r-2)     (wherein X³ and L¹ are as defined above) or -   with their acid anhydrides when the compounds represented by Formula     (r-2) are carboxylic acids or sulfonic acids, in the presence of an     appropriate base, a condensing agent or a diluent, if necessary.

Preparation Method (d) [when A⁵ in Formula (I) is C—(X2-1) or (X2-2), X¹⁰ in Formula (X2-1) or X2-2 is a Hydrogen, m is 1, A⁴ is C—X¹, X¹ and X¹⁰ together Form C₃ alkylene]

A method comprising reacting the compounds represented by Formula (I-d1):

(wherein A¹ to A³ each independently represent nitrogen, C—X¹ or C-T, B¹ to B⁵, G, Q and X³ are as defined above, X¹² independently has the same meaning as X¹ defined above, and n′ represent an integer from 1 to 4)

-   with the compounds represented by Formula (r-1-1) mentioned above or     the compounds represented by Formula (r-1-2) mentioned above, or -   with acid anhydrides of the respective compounds, in the presence of     an appropriate base, a condensing agent or a diluent, if necessary,     and -   further, with the compounds represented by Formula (r-2) mentioned     above, or -   with their acid anhydrides when the compounds represented by Formula     (r-2) are carboxylic acids or sulfonic acids in the presence of an     appropriate base, a condensing agent or a diluent, if necessary.

Preparation Method (e) [when A5 in Formula (I) is C—(X2-1) or (X2-2), X10 in Formula (X2-1) or (X2-2) is hydrogen, m is 1, A4 is C—X1, X1 and X10 together Form C2 alkylene]

A method comprising reacting the compounds represented by Formula (I-e1):

(wherein A¹ to A³, B¹ to B⁵, G, Q, X³ and (X¹²)_(n′)′are as defined above)

-   with the compounds represented by Formula (r-1-1) mentioned above or     the compounds represented by Formula (r-1-2) mentioned above, or -   with acid anhydrides of the respective compounds, in the presence of     an appropriate base, a condensing agent or a diluent, if necessary,     and -   further, with the compounds represented by Formula (r-2) mentioned     above, or with their acid anhydrides when the compounds represented     by Formula (r-2) are carboxylic acids or sulfonic acids in the     presence of an appropriate base, a condensing agent or a diluent, if     necessary.

Preparation Method (f)

A method comprising reacting the compounds represented by Formula (1-f1):

(wherein A¹ to A⁵, B¹ to B⁵ and G are as defined above)

-   with the compounds represented by Formula (r-3):     Q-L²  (r-3)     (wherein Q is as defined above and L² represents fluorine, chlorine,     bromine, a C₁₋₄ alkyl-carbonyloxy group, a C₁₋₄ alkoxy-carbonyloxy     group, an azolyl group, a C₁₋₄ alkylsulfonyloxy group, a C₁₋₄     haloalkylsulfonyloxy group, or an arylsulfonyloxy group) in the     presence of a base or an appropriate diluent, if necessary.

Preparation Method (2) [when G in Formula (I) Represents Sulfur]

A method comprising reacting the compounds represented by Formula (I-g1):

(wherein A¹ to A⁵, B¹ to B⁵ and Q are as defined above)

-   with appropriate sulfurizing reagents in the presence of an     appropriate diluent.

The compounds of Formulas (I-c1), (1-d1), (1-e1), (1-f1) and (1-g1) are encompassed by the compounds of Formula (I) of the present invention.

According to the present invention, carboxamides of Formula (I) of the present invention have a potent pesticidal activity.

In the present specification, “alkyl” represents linear or branched C₁₋₁₂ alkyl such as methyl, ethyl, n- or iso-propyl, n-, iso-, sec- or tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl and n-dodecyl, preferably C₁₋₆ alkyl, and more preferably C₁₋₄ alkyl.

Further, for each alkyl moiety included in a group which includes the alkyl as a part of its constitution, those that are the same as “alkyl” described above can be exemplified.

“Haloalkyl” represents carbon chains in which at least one hydrogen of linear or branched C₁₋₁₂ alkyl, preferably C₁₋₆ alkyl, more preferably C₁₋₄ alkyl is substituted with haloge, for example, CH₂F, CHF₂, CF₃, CF₂Cl, CFCl₂, CF₂Br, CF₂CF₃, CFHCF₃, CH₂CF₃, CFClCF₃, CCl₂CF₃, CF₂CH₃, CF₂CH₂F, CF₂CHF₂, CF₂CF₂Cl, CF₂CF₂Br, CFHCH₃, CFHCHF₂, CFHCHF₂, CHFCF₃, CHFCF₂Cl, CHFCF₂Br, CFClCF₃, CCl₂CF₃, CF₂CF₂CF₃, CH₂CF₂CF₃, CF₂CH₂CF₃, CF₂CF₂CH₃, CHFCF₂CF₃, CF₂CHFCF₃, CF₂CF₂CHF₂, CF₂CF₂CH₂F, CF₂CF₂CF₂Cl, CF₂CF₂CF₂Br, CH(CHF₂)CF₃, CH(CF₃)CF₃, CF(CF₃)CF₃, CF(CF₃)CF₂Br, CF₂CF₂CF₂CF₃, CH(CF₃)CF₂F₃ or CF(CF₃)CF₂CF₃. The haloalkyl also includes perfluoroalkyl in which every substitutable hydrogen on the alkyl is substituted with fluorine. Further, monobromoperfluoroalkyl, which represents an alkyl in which one substitutable hydrogen on the alkyl is substituted with bromo and the rest of every substitutable hydrogen is substituted with fluorine, is also encompassed by “haloalkyl.” The haloalkyl may be further substituted with any substituent.

“Alkoxy” represents alkoxy of linear or branched C₁₋₁₂, preferably C₁₋₆, more preferably C₁₋₄, for example, methoxy, ethoxy, n-propoxy, i-propoxy, n-, iso-, sec- or tert-butoxy, pentyloxy or hexyloxy. The alkoxy may be further substituted with any substituent.

“Halogen” and each halogen moiety included in a group substituted with halogen represent fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine

“Cycloalkyl” represents C₃₋₈ cycloalkyl including cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, preferably C₃₋₇ cycloalkyl, and more preferably C₃₋₆ cycloalkyl.

Further, for each cycloalkyl moiety included in a group which has cycloalkyl as a part of its constitution, those that are the same as “cycloalkyl” described above can be exemplified.

“Halocycloalkyl” represents a cycloalkyl at least one hydrogen on which is substituted by halogen, and examples thereof include fluorocyclopropyl, chlorocyclopropyl, difluorocyclopropyl, dichlorocyclopropyl and undecafluorocyclohexyl.

“Alkenyl” represents C₂₋₁₂ alkenyl, preferably C₂₋₅ alkenyl, such as vinyl, allyl, 1-propenyl, 1-(or 2-, or 3butenyl, 1-pentenyl and the like, and more preferably C₂₋₄ alkenyl.

“Alkynyl” represents C₂₋₁₂ alkynyl, preferably C₂₋₅ alkynyl, such as ethynyl, propargyl, 1-propynyl, butan-3-ynyl, pentan-4-ynyl and the like, and more preferably C₂₋₄ alkynyl.

“Aryl” represents a C₆₋₁₂ aromatic hydrocarbon group, and examples thereof include phenyl, naphthyl, biphenyl, preferably a C₆₋₁₀ aromatic hydrocarbon group, and more preferably a C₆ aromatic hydrocarbon group, i.e., phenyl.

“Heterocycle” represents a 3 to 6-membered heterocyclic group having, as a hetero atom, at least one of N, O and S. In preferred embodiments, a heterocycle refers to a 3, a 5 or a 6 membered heterocyclic group. “Heterocycle” also represents a fused heterocyclic group which may be a benzo-fused heterocycle. Further, the carbon atom in the heterocycle may be substituted with oxo or thioxo.

Specific examples of the heterocycle include pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, aziridinyl, oxiranyl, thiiranyl, azetidinyl, oxetanyl, thietanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, tetrahydropyranyl, tetrahydrothiopyranyl (as examples of a saturated heterocycle), dihydropyrrolyl, dihydroisoxazolyl, dihydropyrazolyl, dihydrooxazolyl, dihydrothiazolyl (as examples of a partially saturated heterocycle), furyl, thienyl, pyrrolyl, isoxazolyl, pyrazolyl, oxazolyl, isothiazolyl, thiazolyl, imidazolyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, indolyl, benzoxazolyl, benzothiazolyl, quinolyl and the like. Furthermore, the heterocycle may be substituted with any substituent.

Examples of the substituent described in the expression “may be substituted with any substituent” include amino, hydroxy, oxo, thioxo, halogen, nitro, cyano, isocyano, mercapto, isothiocyanate, carboxy, carboamide, SF₅, aminosulfonyl, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, monoalkylamino, dialkylamino, N-alkylcarbonyl-amino, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, cycloalkenyloxy, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, aryloxycarbonyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, arylcarbonyl, alkylthio, cycloalkylthio, alkenylthio, cycloalkenylthio, alkynylthio, alkylsulfenyl, alkylsulfinyl, alkylsulfinyl including isomers, alkylsulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylphosphinyl, alkylphosphonyl, alkylphosphinyl including isomers, alkylphosphonyl including isomers, N-alkyl-aminocarbonyl, N,N-dialkyl-aminocarbonyl, N-alkylcarbonyl-aminocarbonyl, N-alkylcarbonyl-N-alkylaminocarbonyl, aryl, aryloxy, benzyl, benzyloxy, benzylthio, arylthio, arylamino, benzylamino, heterocycle, trialkylsilyl, alkoxyalkyl, alkylthioalkyl, alkylthioalkoxy, alkoxyalkoxy, phenethyl, benzyloxy, haloalkyl, haloalkoxy, haloalkylthio, haloalkylcarbonyl, haloalkoxycarbonyl, haloalkoxyalkoxy, haloalkoxyalkylthio, haloalkoxyalkylcarbonyl and haloalkoxyalkyl, and preferably chloro, fluoro, bromo, iodo, amino, nitro, cyano, hydroxy, thio and carboxy.

In a preferred embodiment of the present invention, at least one of X¹, X², T or J³ represents a nitrogen-containing heterocycle, i.e., the core of the heterocycle contains only C and N. More preferably, the nitrogen-containing heterocycle is a 5 membered heterocycle.

In an even more preferred embodiment of the present invention, at least one of X¹, X², T or J³ is selected from one of the following substituents W1-W9:

wherein Z each independently represents hydrogen, halogen, nitro, cyano, hydroxy, thio, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylthio, C₁₋₆ haloalkylsulfinyl or C₁₋₆ haloalkylsulfonyl, and k represents an integer from 1 to 4. In a preferred embodiments Z is hydrogen.

In another preferred embodiment of the present invention, all alkyl or alkyl-containing substituents (e.g. haloalkyl, alkyl-O— etc.) of compounds of the present invention are C₁₋₆ alkyl or C₁₋₆ alkyl-containing substituents, respectively, more preferably said alkyl or alkyl-containing substituents are C₁₋₄ alkyl or C₁₋₄ alkyl-containing-substituents, respectively.

In yet another preferred embodiment, T represents any one of the substituents represented by the following Formulae (X2-1) to (X2-4):

wherein

-   -   X³, X⁵ and G independently have the same meaning as X³, X⁵ and G         defined above, respectively;     -   X⁹, X¹⁰ and X¹¹ each independently have the same meaning as X³,         X⁴ and X⁵ defined above, respectively,     -   X⁹ and X¹⁰ may form a 3- to 8-membered carbon ring or         heterocycle, together with the carbon atom to which they are         bonded,     -   X⁹ and X⁵, X¹⁰ and X⁵, or X¹¹ and X⁵ may together form C₁₋₄         alkylene;     -   R12 and R13 have the same meaning as X⁹ and X¹⁰, respectively,     -   R14 has the same meaning as X³ described above, and     -   R15 represents hydrogen;

Among the compounds represented by Formula (I) of the present invention, the following compounds may be referred to as preferred compounds.

The compounds represented by formula (I) wherein

-   A¹, A², A³, A⁴ and A⁵ each independently represent nitrogen, C—X¹ or     C-T, provided that at least one of A¹, A², A³, A⁴ and A⁵ is C-T; -   B¹, B², B³, B⁴ and B⁵ each independently represent nitrogen, C—X² or     C-J, provided that at least one of B¹, B², B³, B⁴ and B⁵ is C-J; -   G represents oxygen or sulfur; -   Q represents hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, (C₁₋₆     alkyl)carbonyl, (C₁₋₆ haloalkyl)carbonyl, (C₁₋₆ alkoxy)carbonyl or     (C₁₋₆ haloalkoxy)carbonyl; -   X¹ and X² each independently represent hydrogen, cyano, halogen,     nitro, hydroxy, mercapto, amino, formyl, oxide, C₁₋₆ alkyl, C₁₋₆     haloalkyl, aryl-(C₁₋₆)alkyl, heterocyclyl-(C₁₋₆)alkyl, C₁₋₆     alkyl-O—, C₁₋₆ alkyl-NH—, C₁₋₆ alkyl-S—, C₁₋₆ alkyl-S(O)—, C₁₋₆     alkyl-S(O)₂—, C₁₋₆ alkyl-S(O)₂O—, C₁₋₆ haloalkyl-O—, C₁₋₆     haloalkyl-NH—, C₁₋₆ haloalkyl-S—, C₁₋₆ haloalkyl-S(O)—, C₁₋₆     haloalkyl-S(O)₂—, C₁₋₆ haloalkyl-S(═O)₂O—, aryl-O—, aryl-NH—,     aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—,     heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—,     heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₆ alkyl-O—(C₁₋₆)alkyl,     C₁₋₆ alkyl-NH—(C₁₋₆)alkyl, C₁₋₆ alkyl-S—(C₁₋₆)alkyl, C₁₋₆     alkyl-S(O)—(C₁₋₆)alkyl, C₁₋₆ alkyl-S(O)₂—(C₁₋₆)alkyl, C₁₋₆     alkyl-S(O)₂O—(C₁₋₆)alkyl, C₁₋₆ haloalkyl-O—(C₁₋₆)alkyl, C₁₋₆     haloalkyl-NH—(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S—(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S(O)—(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S(O)₂—(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S(O)₂O—(C₁₋₆)alkyl, aryl-O—(C₁₋₆)alkyl,     aryl-NH—(C₁₋₆)alkyl, aryl-S—(C₁₋₆)alkyl, aryl-S(O)—(C₁₋₆)alkyl,     aryl-S(O)₂—(C₁₋₆)alkyl, aryl-S(O)₂O—(C₁₋₆)alkyl,     heterocyclyl-O—(C₁₋₆)alkyl, heterocyclyl-NH—(C₁₋₆)alkyl,     heterocyclyl-S—(C₁₋₆)alkyl, heterocyclyl-S(O)—(C₁₋₆)alkyl,     heterocyclyl-S(O)₂—(C₁₋₆)alkyl, heterocyclyl-S(O)₂O—(C₁₋₆)alkyl,     C₃₋₇ cycloalkyl, C₃₋₇ cycloalkyl-(C₁₋₆)alkyl-, C₃₋₇ halocycloalkyl,     C₃₋₇ halocycloalkyl-(C₁₋₆)alkyl-, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl,     C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, di(C₁₋₆ alkyl)amino, di(C₁₋₆     haloalkyl)amino, C₃₋₁₈ trialkylsilyl, hydroxyimino(C₁₋₆)alkyl, C₁₋₆     alkyl-O—N═(C₁₋₆)alkyl, C₁₋₆ alkyl-NH—N═(C₁₋₆)alkyl, C₁₋₆     alkyl-S—N═(C₁₋₆)alkyl, C₁₋₆ alkyl-S(O)—N═(C₁₋₆)alkyl, C₁₋₆     alkyl-S(O)₂—N═(C₁₋₆)alkyl, C₁₋₆ alkyl-S(O)₂O—N═(C₁₋₆)alkyl, C₁₋₆     haloalkyl-O—N═(C₁₋₆)alkyl, C₁₋₆ haloalkyl-NH—N═(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S—N═(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S(O)—N═(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S(O)₂—N═(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S(O)₂O—N═(C₁₋₆)alkyl,     (C₁₋₆ alkoxy)carbonyl, (C₁₋₆ haloalkoxy)carbonyl, (C₃₋₇     cycloalkoxy)carbony, (C₃₋₇ halocycloalkoxy)carbony, C₃₋₇     cycloalkyl-(C₁₋₆ alkoxy)carbony, C₃₋₇ halocycloalkyl-(C₁₋₆     alkoxy)carbony, (C₁₋₆ alkyl)carbonyl, (C₁₋₆ haloalkyl)carbonyl,     (C₃₋₇ cycloalkyl)carbonyl, (C₃₋₇ halocycloalkyl)carbonyl, C₃₋₇     cycloalkyl-(C₁₋₆)alkyl-carbonyl, (C₃₋₇     halocycloalkyl)-(C₁₋₆)alkyl-carbonyl, an aryl group, sulfur     pentafluoride, one of the substituents represented by the following     Formulae (X1-1) to (X1-5):

-   -   wherein G independently has the same meaning as G described         above;         or

-   X¹ and X² each independently represent a heterocyclic group     represented by any one of W1 to W9 as described above;

-   X³, X⁴ and X⁵ each independently represent hydrogen, cyano, halogen,     nitro, hydroxy, mercapto, amino, formyl, C₁₋₆ alkyl, C₁₋₆ haloalkyl,     aryl-(C₁₋₆)alkyl, heterocyclyl-(C₁₋₆)alkyl, C₁₋₆ alkyl-O—, C₁₋₆     alkyl-NH—, C₁₋₆ alkyl-S—, C₁₋₆ alkyl-S(O)—, C₁₋₆ alkyl-S(O)₂—, C₁₋₆     alkyl-S(O)₂O—, C₁₋₆ haloalkyl-O—, C₁₋₆ haloalkyl-NH—, C₁₋₆     haloalkyl-S—, C₁₋₆ haloalkyl-S(O)—, C₁₋₆ haloalkyl-S(O)₂—, C₁₋₆     haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—,     aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—,     heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—,     heterocyclyl-S(O)₂O—, C₁₋₆ alkyl-O—(C₁₋₆)alkyl, C₁₋₆     alkyl-NH—(C₁₋₆)alkyl, C₁₋₆ alkyl-S—(C₁₋₆)alkyl, C₁₋₆     alkyl-S(O)—(C₁₋₆)alkyl, C₁₋₆ alkyl-S(O)₂—(C₁₋₆)alkyl, C₁₋₆     alkyl-S(O)₂O—(C₁₋₆)alkyl, C₁₋₆ haloalkyl-O—(C₁₋₆)alkyl, C₁₋₆     haloalkyl-NH—(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S—(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S(O)—(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S(O)₂—(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S(O)₂O—(C₁₋₆)alkyl, aryl-O—(C₁₋₆)alkyl,     aryl-NH—(C₁₋₆)alkyl, aryl-S—(C₁₋₆)alkyl, aryl-S(O)—(C₁₋₆)alkyl,     aryl-S(O)₂—(C₁₋₆)alkyl, aryl-S(O)₂O—(C₁₋₆)alkyl,     heterocyclyl-O—(C₁₋₆)alkyl, heterocyclyl-NH—(C₁₋₆)alkyl,     heterocyclyl-S—(C₁₋₆)alkyl, heterocyclyl-S(O)—(C₁₋₆)alkyl,     heterocyclyl-S(O)₂—(C₁₋₆)alkyl, heterocyclyl-S(O)₂O—(C₁₋₆)alkyl,     C₃₋₇ cycloalkyl, C₃₋₇ cycloalkyl-(C₁₋₆)alkyl-, C₃₋₇ halocycloalkyl,     C₃₋₇ halocycloalkyl-(C₁₋₆)alkyl-, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl,     C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, di(C₁₋₆ alkyl)amino, di(C₁₋₆     haloalkyl)amino, C₃₋₁₈ trialkylsilyl, hydroxyimino(C₁₋₆)alkyl, C₁₋₆     alkyl-O—N═(C₁₋₆)alkyl, C₁₋₆ alkyl-NH—N═(C₁₋₆)alkyl, C₁₋₆     alkyl-S—N═(C₁₋₆)alkyl, C₁₋₆ alkyl-S(O)—N═(C₁₋₆)alkyl, C₁₋₆     alkyl-S(O)₂—N═(C₁₋₆)alkyl, C₁₋₆ alkyl-S(O)₂O—N═(C₁₋₆)alkyl, C₁₋₆     haloalkyl-O—N═(C₁₋₆)alkyl, C₁₋₆ haloalkyl-NH—N═(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S—N═(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S(O)—N═(C₁₋₆)alkyl, C₁₋₆     haloalkyl-S(O)₂—N═(C₁₋₆)alkyl, C₁₋₆ haloalkyl-S(O)₂O—N═(C₁₋₆)alkyl,     (C₁₋₆ alkoxy)carbonyl, (C₁₋₆ haloalkoxy)carbonyl, (C₃₋₇     cycloalkoxy)carbony, (C₃₋₇ halocycloalkoxy)carbony, C₃₋₇     cycloalkyl-(C₁₋₆ alkoxy)carbony, C₃₋₇ halocycloalkyl-(C₁₋₆     alkoxy)carbony, (C₁₋₆ alkyl)carbonyl, (C₁₋₆ haloalkyl)carbonyl,     (C₃₋₇ cycloalkyl)carbonyl, (C₃₋₇ halocycloalkyl)carbonyl, C₃₋₇     cycloalkyl-(C₁₋₆)alkyl-carbonyl, C₃₋₇     halocycloalkyl-(C₁₋₆)alkyl-carbonyl, aryl-carbonyl,     heterocyclyl-carbonyl, aryl-(C₁₋₆)alkyl-carbonyl,     heterocyclyl-(C₁₋₆)alkyl-carbonyl, sulfur pentafluoride, an aryl     group or a heterocyclic group,

-   X³ and X⁴ may form a heterocycle together with the nitrogen atom,     carbon atom, oxygen atom or sulfur atom to which they are bonded,

-   X³ and X⁵ may form a heterocycle together with the nitrogen atom,     carbon atom, oxygen atom or sulfur atom to which they are bonded;

-   X⁶ each independently represents hydrogen, C₁₋₆ alkyl, C₁₋₆     haloalkyl, C₃₋₇ cycloalkyl, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, an aryl     group, a heterocyclic group, aryl-(C₁₋₆)alkyl or     heterocyclyl-(C₁₋₆)alkyl;

-   X⁷ each independently represents hydrogen, nitro, cyano, formyl,     X⁸-carbonyl or X⁸-oxycarbonyl,     -   wherein X⁸ independently has the same meaning as X⁶ described         above;

-   J each independently represents C₁₋₆ haloalkyl, C₁₋₆ haloalkyl-O—,     C₁₋₆ haloalkyl-S—, C₁₋₆ haloalkyl-S(═O)—, C₁₋₆ haloalkyl-S(═O)₂—,     C₃₋₇ halocycloalkyl, —C(J¹)(J²)(J³) or —C(J¹)(J²)(OJ⁴),     -   wherein J¹ and J² each independently represent C₁₋₆ haloalkyl,     -   J³ independently represents any one of the above W1 to W9;     -   J⁴ represents hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆         alkylsulfonyl, C₁₋₆ haloalkylsulfonyl, arylsulfonyl, an aryl         group or a heterocyclic group;

-   T represents any one of the substituents represented by W1 to W9     mentioned above or any one of the substituents represented by the     following Formulae (X2-1) to (X2-4):

wherein

-   -   m each independently represents an integer of 1 to 4;     -   X³, X⁵ and G independently have the same meaning as X³, X⁵ and G         defined above, respectively;     -   X⁹, X¹⁰ and X¹¹ each independently have the same meaning as X³,         X⁴ and X⁵ defined above, respectively,     -   X⁹ and X¹⁰ may form a 3- to 8-membered carbon ring or         heterocycle, together with the carbon atom to which they are         bonded,     -   X⁹ and X⁵, X¹⁰ and X⁵, or X¹¹ and X⁵ may together form C₁₋₄         alkylene     -   R12 and R13 have the same meaning as X⁹ and X¹⁰, respectively,     -   R14 has the same meaning as X³ described above, and     -   R15 represents hydrogen;

-   when A¹, A², A³, A⁴ or A⁵ is C-T and T represents any one of the     substituents represented by Formulae (X2-1) to (X2-4), then X⁹, X¹⁰,     X¹¹ or X³ in T may form C₁₋₄ alkylene together with X¹ if A¹, A²,     A³, A⁴ or A⁵ that is adjacent to the carbon atom to which T in C-T     is bonded is C—X¹, and one —CH₂— at any position in the alkylene may     be replaced by —O—, —S— or —NH—;

-   when both A¹ and A² represent C—X¹ then X¹'s in the C—X¹'s may form     a 5- to 6-membered saturated or unsaturated carbon ring or     heterocycle, together with the carbon atoms to which X¹'s in C—X¹'s     are bonded, and when both A³ and A⁴ represent C—X¹, then X¹'s in the     C—X¹'s may form a 5- to 6-membered saturated or unsaturated carbon     ring or heterocycle, together with the carbon atoms to which X¹'s in     C—X¹'s are bonded; and

-   each substituent defined above may be further substituted with any     substituent.

Among the compounds represented by formula (I) the following compounds are especially suitable.

The compounds of formula (I) wherein

-   A¹, A², A³, A⁴ and A⁵ each independently represent nitrogen, C—X¹ or     C-T, provided that at least one of A¹, A², A³, A⁴ and A⁵ is C-T; -   B¹, B², B³, B⁴ and B⁵ each independently represent nitrogen, C—X² or     C-J, provided that at least one of B′, B², B³, B⁴ and B⁵ is C-J; -   G represents oxygen or sulfur; -   Q represents hydrogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄     alkyl)carbonyl, (C₁₋₄ haloalkyl)carbonyl, (C₁₋₄ alkoxy)carbonyl or     (C₁₋₄ haloalkoxy)carbonyl; -   X¹ and X² each independently represent hydrogen, cyano, halogen,     nitro, hydroxy, mercapto, amino, formyl, oxide, C₁₋₄ alkyl, C₁₋₄     haloalkyl, aryl-(C₁₋₄)alkyl, heterocyclyl-(C₁₋₄ alkyl, C₁₋₄     alkyl-O—, C₁₋₄ alkyl-NH—, C₁₋₄ alkyl-S—, C₁₋₄ alkyl-S(O)—, C₁₋₄     alkyl-S(O)₂—, C₁₋₄ alkyl-S(O)₂O—, C₁₋₄ haloalkyl-O—,     C₁₋₄haloalkyl-NH—, C₁₋₄ haloalkyl-S—, C₁₋₄ haloalkyl-S(O)—, C₁₋₄     haloalkyl-S(O)₂—, C₁₋₄ haloalkyl-S(═O)₂O—, aryl-O—, aryl-NH—,     aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—,     heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—,     heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₄ alkyl-O—(C₁₋₄)alkyl,     C₁₋₄ alkyl-NH—(C₁₋₄)alkyl, C₁₋₄ alkyl-S—(C₁₋₄)alkyl, C₁₋₄     alkyl-S(O)—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂—(C₁₋₄)alkyl, C₁₋₄     alkyl-S(O)₂O—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-O—(C₁₋₄ alkyl, C₁₋₄     haloalkyl-NH—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S—(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S(O)—(C₁₋₄ alkyl, C₁₋₄ haloalkyl-S(O)₂—(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S(O)₂O—(C₁₋₄)alkyl, aryl-O—(C₁₋₄)alkyl,     aryl-NH—(C₁₋₄)alkyl, aryl-S—(C₁₋₄)alkyl, aryl-S(O)—(C₁₋₄)alkyl,     aryl-S(O)₂—(C₁₋₄)alkyl, aryl-S(O)₂O—(C₁₋₄)alkyl,     heterocyclyl-O—(C₁₋₄)alkyl, heterocyclyl-NH—(C₁₋₄)alkyl,     heterocyclyl-S—(C₁₋₄ alkyl, heterocyclyl-S(O)—(C₁₋₄ alkyl,     heterocyclyl-S(O)₂—(C₁₋₄)alkyl, heterocyclyl-S(O)₂O—(C₁₋₄)alkyl,     C₃₋₆ cycloalkyl, C₃₋₆ cycloalkyl-(C₁₋₄)alkyl-, C₃₋₆ halocycloalkyl,     C₃₋₆ halocycloalkyl-(C₁₋₄)alkyl-, C₂ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄     alkynyl, C₂₋₄ haloalkynyl, di(C₁₋₄ alkyl)amino, di(C₁₋₄     haloalkyl)amino, C₃₋₁₂ trialkylsilyl, hydroxyimino(C₁₋₄)alkyl, C₁₋₄     alkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄     alkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄     alkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂O—N═(C₁₋₄)alkyl, C₁₋₄     haloalkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂O—N═(C₁₋₄)alkyl,     (C₁₋₄ alkoxy)carbonyl, (C₁₋₄ haloalkoxy)carbonyl, (C₃₋₆     cycloalkoxy)carbony, (C₃₋₆ halocycloalkoxy)carbony, C₃₋₆     cycloalkyl-(C₁₋₄ alkoxy)carbony, C₃₋₆ halocycloalkyl-(C₁₋₄     alkoxy)carbony, (C₁₋₄ alkyl)carbonyl, (C₁₋₄ haloalkyl)carbonyl,     (C₃₋₆ cycloalkyl)carbonyl, (C₃₋₆ halocycloalkyl)carbonyl, C₃₋₆     cycloalkyl-(C₁₋₄ alkyl-carbonyl, (C₃₋₆     halocycloalkyl)-(C₁₋₄)alkyl-carbonyl, an aryl group, sulfur     pentafluoride, one of the substituents represented by the following     Formulae (X1-1) to (X1-5):

wherein G independently has the same meaning as G described above; or

-   X¹ and X² each independently represent a heterocyclic group     represented by any one of W1 to W9; -   X³, X⁴ and X⁵ each independently represent hydrogen, cyano, halogen,     nitro, hydroxy, mercapto, amino, formyl, C₁₋₄ alkyl, C₁₋₄ haloalkyl,     aryl-(C₁₋₄)alkyl, heterocyclyl-(C₁₋₄)alkyl, C₁₋₄ alkyl-O—, C₁₋₄     alkyl-NH—, C₁₋₄ alkyl-S—, C₁₋₄ alkyl-S(O)—, C₁₋₄ alkyl-S(O)₂—, C₁₋₄     alkyl-S(O)₂O—, C₁₋₄ haloalkyl-O—, C₁₋₄ haloalkyl-NH—, C₁₋₄     haloalkyl-S—, C₁₋₄haloalkyl-S(O)—, C₁₋₄haloalkyl-S(O)₂—, C₁₋₄     haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—,     aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—,     heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—,     heterocyclyl-S(O)₂O—, C₁₋₄ alkyl-O—(C₁₋₄)alkyl, C₁₋₄     alkyl-NH—(C₁₋₄)alkyl, C₁₋₄ alkyl-S—(C₁₋₄)alkyl, C₁₋₄     alkyl-S(O)—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂—(C₁₋₄)alkyl, C₁₋₄     alkyl-S(O)₂O—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-O—(C₁₋₄)alkyl, C₁₋₄     haloalkyl-NH—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S—(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S(O)—(C₁₋₄ alkyl, C₁₋₄ haloalkyl-S(O)₂—(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S(O)₂O—(C₁₋₄)alkyl, aryl-O—(C₁₋₄)alkyl,     aryl-NH—(C₁₋₄)alkyl, aryl-S—(C₁₋₄)alkyl, aryl-S(O)—(C₁₋₄)alkyl,     aryl-S(O)₂—(C₁₋₄)alkyl, aryl-S(O)₂O—(C₁₋₄)alkyl,     heterocyclyl-O—(C₁₋₄)alkyl, heterocyclyl-NH—(C₁₋₄)alkyl,     heterocyclyl-S—(C₁₋₄)alkyl, heterocyclyl-S(O)—(C₁₋₄ alkyl,     heterocyclyl-S(O)₂—(C₁₋₄)alkyl, heterocyclyl-S(O)₂O—(C₁₋₄)alkyl,     C₃₋₆ cycloalkyl, C₃₋₆ cycloalkyl-(C₁₋₄)alkyl-, C₃₋₆ halocycloalkyl,     C₃₋₆ halocycloalkyl-(C₁₋₄)alkyl-, C₂ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄     alkynyl, C₂₋₄ haloalkynyl, di(C₁₋₄ alkyl)amino, di(C₁₋₄     haloalkyl)amino, C₃₋₁₂ trialkylsilyl, hydroxyimino(C₁₋₄)alkyl, C₁₋₄     alkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄     alkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄     alkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂O—N═(C₁₋₄)alkyl, C₁₋₄     haloalkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄     haloalkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂O—N═(C₁₋₄)alkyl,     (C₁₋₄ alkoxy)carbonyl, (C₁₋₄ haloalkoxy)carbonyl, (C₃₋₆     cycloalkoxy)carbony, (C₃₋₆ halocycloalkoxy)carbony, C₃₋₆     cycloalkyl-(C₁₋₄ alkoxy)carbony, C₃₋₆ halocycloalkyl-(C₁₋₄     alkoxy)carbony, (C₁₋₄ alkyl)carbonyl, (C₁₋₄ haloalkyl)carbonyl,     (C₃₋₆ cycloalkyl)carbonyl, (C₃₋₆ halocycloalkyl)carbonyl, C₃₋₆     cycloalkyl-(C₁₋₄ alkyl-carbonyl, C₃₋₆ halocycloalkyl-(C₁₋₄     alkyl-carbonyl, aryl-carbonyl, heterocyclyl-carbonyl,     aryl-(C₁₋₄)alkyl-carbonyl, heterocyclyl-(C₁₋₄)alkyl-carbonyl, sulfur     pentafluoride, an aryl group or a heterocyclic group, -   X³ and X⁴ may form a heterocycle together with the nitrogen atom,     carbon atom, oxygen atom or sulfur atom to which they are bonded, -   X³ and X⁵ may form a heterocycle together with the nitrogen atom,     carbon atom, oxygen atom or sulfur atom to which they are bonded; -   X⁶ each independently represents hydrogen, C₁₋₄ alkyl, C₁₋₄     haloalkyl, C₃₋₆ cycloalkyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, an aryl     group, a heterocyclic group, aryl-(C₁₋₄)alkyl or     heterocyclyl-(C₁₋₄)alkyl; -   X⁷ each independently represents hydrogen, nitro, cyano, formyl,     X⁸-carbonyl or X⁸-oxycarbonyl,     -   wherein X⁸ independently has the same meaning as X⁶ described         above; -   J each independently represents C₁₋₄ haloalkyl, C₁₋₄ haloalkyl-O—,     C₁₋₄ haloalkyl-S—, C₁₋₄ haloalkyl-S(═O)—, C₁₋₄ haloalkyl-S(═O)₂—,     C₃₋₆ halocycloalkyl, —C(J¹)(J²)(J³) or —C (J¹)(J²)(OJ⁴),     -   wherein J¹ and J² each independently represent C₁₋₄ haloalkyl,     -   J³ independently represents any one of the above W1 to W9;     -   J⁴ represents hydrogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄         alkylsulfonyl, C₁₋₄ haloalkylsulfonyl, arylsulfonyl, an aryl         group or a heterocyclic group; -   T represents any one of the substituents represented by W1 to W9     mentioned above or any one of the substituents represented by the     following Formulae (X2-1) to (X2-4):

wherein

-   m each independently represents an integer of 1 to 4; -   X³, X⁵ and G independently have the same meaning as X³, X⁵ and G     defined above, respectively; -   X⁹, X¹⁰ and X¹¹ each independently have the same meaning as X³, X⁴     and X⁵ defined above, respectively, -   X⁹ and X¹⁰ may form a 3- to 8-membered carbon ring or heterocycle,     together with the carbon atom to which they are bonded, -   X⁹ and X⁵, X¹⁰ and X⁵, or X¹¹ and X⁵ may together form C₁₋₄ alkylene     -   R12 and R13 have the same meaning as X⁹ and X¹⁰, respectively,     -   R14 has the same meaning as X³ described above, and     -   R15 represents hydrogen; -   when A¹, A², A³, A⁴ or A⁵ is C-T and T represents any one of the     substituents represented by Formulae (X2-1) to (X2-4), then X9, X¹⁰,     X¹¹ or X³ in T may form C₁₋₄ alkylene together with X¹ if A¹, A²,     A³, A⁴ or A⁵ that is adjacent to the carbon atom to which T in C-T     is bonded is C—X¹, and one —CH₂— at any position in the alkylene may     be replaced by —O—, —S— or —NH—; -   when both A¹ and A² represent C—X¹ then X¹'s in the C—X¹'s may form     a 5- to 6-membered saturated or unsaturated carbon ring or     heterocycle, together with the carbon atoms to which X¹'s in C—X¹'s     are bonded, and when both A³ and A⁴ represent C—X¹, then X¹'s in the     C—X¹'s may form a 5- to 6-membered saturated or unsaturated carbon     ring or heterocycle, together with the carbon atoms to which X¹'s in     C—X¹'s are bonded; and -   each substituent defined above may be further substituted with any     substituent.

In another preferred embodiment of the present invention, the compounds are preferred wherein in formula (I) the grouping

(Wherein the bond marked by (*) bonds to the carbon atom marked by (#) of the grouping

stands for a grouping selected among LH-1 to LH-13

wherein W represents any one of W1 to W9 described above, R7, R8, R9, R10, R11 and X¹² each independently has the same meaning as X¹ defined above, R12 and R13 have the same meaning as X⁹ and X¹⁰ described above respectively, R14 has the same meaning as X³ described above, R15 represents hydrogen or has the same meaning as —C (=G)-X⁵; G and X⁵ are as defined above, and n′ represent an integer from 1 to 4.

Among the compounds of the Formula (I) of the present invention, the compounds are preferred wherein in formula (I) the grouping

(Wherein the bond marked by (*) bonds to the nitrogen atom marked by (#) of the grouping

stands for a grouping:

wherein,

-   R1, R2, R4 and R5 each independently has the same meaning as X²     defined above, more preferably each independently represent     hydrogen, cyano, halogen, oxygen, C₁₋₄ alkyl, C₁₋₄haloalkyl,     C₁₋₄haloalkyl-O—, or haloalkyl-S(O)₂—, -   J each independently represents C₁₋₄ perfluoroalkyl, C₁₋₄     perfluoroalkyl-O—, C₁₋₄ monobromoperfluoroalkyl, C₁₋₄     perfluoroalkyl-S(O)₂—, C₃₋₆ perfluorocycloalkyl, —C(J¹)(J²)(J³) or     —C(J¹)(J²)(OJ⁴),     -   J¹ and J² each independently represent C₁₋₄ perfluoroalkyl,     -   J³ represents W2:

-   -   Z each independently represents hydrogen or halogen,     -   k is 3,     -   J⁴ represents C₁₋₄ alkyl, or phenyl; and

-   each group defined above may be further substituted with any     substituent.

The following groups of the novel carboxamides are also preferred, and in any case they are understood as subgroups of the compounds of the Formula (I) described above.

Group 1: Carboxamides represented by Formula (I-I):

wherein G, Q and J are as defined above, W represents any one of W1 to W9 described above, R1, R2, R4 and R5 each independently has the same meaning as X² defined above, and R7, R8, R9 and R10 each independently has the same meaning as X¹ defined above.

Group 2: Carboxamides represented by Formula (I-II):

wherein W, G, Q, J, R1, R2, R4, R5, R9, R10 and (X¹²)_(n′) are as defined above.

Group 3: Carboxamides represented by Formula (I-III):

wherein W, G, Q, J, R1, R2, R4, R5, R8, R9 and R10 are as defined above.

Group 4: Carboxamides represented by Formula (I-IV)

wherein W, G, Q, J, R1, R2, R4, R5, R7, R9 and R10 are as defined above.

Group 5: Carboxamides represented by Formula (I-V):

wherein G, Q, J, R1, R2, R4, R5, R7, R8, R9, R10 and m are as defined above, R12 and R13 have the same meaning as X⁹ and X¹⁰ described above, respectively, R14 has the same meaning as X³ described above, R15 represents hydrogen or has the same meaning as —C (=G)-X⁵, and G and X⁵ are as defined above.

Group 6: Carboxamides represented by Formula (I-VI):

wherein G, Q, J, R1, R2, R4, R5, R9, R10, R12, R13, R14, R15, (X¹²)_(n′) and m are as defined above.

Group 7: Carboxamides represented by Formula (I-VII):

wherein G, Q, J, R1, R2, R4, R5, R8, R9, R10, R12, R13, R14, R15 and m are as defined above.

Group 8: Carboxamides represented by Formula (I-VIII):

wherein G, Q, J, R1, R2, R4, R5, R7, R9, R10, R12, R13, R14, R15 and m are as defined above.

Group 9: Carboxamides represented by Formula (I-IX):

wherein G, Q, J, R1, R2, R4, R5, R7, R9, R10, R12, R13, R14, R15 and (X¹²)_(n′) are as defined above, and n represents 0, 1 or 2.

Group 10: Carboxamides represented by Formula (I-X):

wherein G, Q, J, R1, R2, R4, R5, R7, R9, R10, R12, R13, R14, R15 and X¹² are as defined above, and n represents 0, 1 or 2.

Group 11: Carboxamides represented by Formula (I-XI):

wherein W, G, Q, J, R1, R2, R4, R5, R7, R9, R10, R12, R13, R14, R15 and m are as defined above.

Group 12: Carboxamides represented by Formula (I-XII):

wherein W, G, Q, J, R1, R2, R4, R5, R7, R9, R10, R12, R13, R14, R15 and m are as defined above.

Group 13: Carboxamides represented by Formula (I-XIII):

wherein G, Q and J are as defined above; W represents any one of the above W1 to W9; R1, R2, R4 and R5 independently have the same meaning as X² above; and R7, R9, R10 and R11 independently have the same meaning as X¹ above.

Herein, the carboxamides of Formula (I) and the carboxamides of Groups 1 to 13 satisfying the followings are preferable:

-   J each independently represents C₁₋₄ perfluoroalkyl, C₁₋₄     monobromoperfluoroalkyl, C₃₋₆ perfluorocycloalkyl, —C(J¹)(J²)(J³) or     —C(J¹)(J²)(OJ⁴),     -   J¹ and J² each independently represent C₁₋₄ perfluoroalkyl,     -   J³ represents any one of the substituents represented by         Formulae W1 to W9 as described above,     -   J⁴ represents C₁₋₄ alkyl, C₁₋₄ haloalkyl or a phenyl group, and -   each group defined above may be substituted with any substituent.

The compounds of Formula (I) of the present invention may have an asymmetric carbon, and therefore optical isomers are included in such compounds.

Preparation method (a) can be represented by the following reaction formula when 4-(1H-1,2,4-triazolo-1-yl)benzoyl chloride and 2,6-dibromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)aniline are used as startnig materials, for example.

Preparation method (b) can be represented by the following reaction formula when N-[2-ethyl-4-(1, 1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluoro-3-nitrobenzamide and 1H-1,2,4-triazole are used as starting materials, for example.

Preparation method (c) can be represented by the following reaction formula when 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benzamide and acetic anhydride are used as starting materials, for example.

Preparation method (d) can be represented by the following reaction formula when 5-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-5,6,7,8-tetrahydronaphthalene-2-carboxamide and acetic acid are used as starting materials, for example.

Preparation method (e) can be represented by the following reaction formula when 1-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-indane-5-carboxamide and acetic acid are used as starting materials, for example.

Preparation method (f) can be represented by the following reaction formula when N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide and methyl iodide are used as starting materials, for example.

Preparation method (g) can be represented by the following reaction formula when N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide and Lawesson reagent are used as starting materials, for example.

Explanation on the respective Preparation methods and intermediates will be provided below.

The compounds of Formula (II) which are starting materials in Preparation method (a) are publicly known and their representative examples are as follows:

-   4-(1H-pyrrol-1-yl)benzoyl chloride, -   4-(1H-pyrazol-1-yl)benzoyl chloride, -   3-chloro-4-(1H-pyrazol-1-yl)benzoyl chloride, -   4-(1H-imidazol-1-yl)benzoyl chloride, -   4-(1H-1,2,4-triazol-1-yl)benzoyl chloride, -   4-(1H-tetrazol-1-yl)benzoyl chloride, -   4-cyano-3-fluorobenzoyl chloride and the like.

When L¹ of Formula (II) represents hydroxy in the starting materials for Preparation method (a), they can be reacted with the compounds of Formula (III) in the presence of a condensing agent.

As the condensing agent, 1,3-dicyclohexylcarbodiimide (DCC), 1-ethyl-3-(3′-dimethylaminopropyl)-carbodiimide hydrochloride (WSCI), carbonyldiimidazole (CDI), diethyl phosphocyanate (DEPC), 2-chloro-1-methylpyridinium iodide (Mukaiyama reagent), etc. can be used for the reaction.

When L¹ of Formula (II) represents hydroxy in the starting materials for Preparation method (a), L¹ can be easily converted to an appropriate substituent by several methods including, pre-reacting with a chlorination agent, such as thionyl chloride, oxalyl chloride or phosphorous pentachloride, reacting with an organic acid halide, such as pyvaloyl chloride, or reacting with carbonyldiimidazole or sulfonylimidazole and the like.

Some of the compounds of Formula (III) as starting materials for Preparation method (a) are known and they can be synthesized according to the methods described in US 2002/0198399A1, WO 2005/021488A1, WO 2005/073165A1, WO 2006/024412A2 or Japanese Patent Application No. 2009-172800. Their representative examples are as follows:

-   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylaniline, -   2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline, -   2,6-diethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)aniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-ethylaniline, -   2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)aniline, -   2,6-dibromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-diiodoaniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-(trifluoromethyl)aniline, -   2-chloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-(trifluoromethyl)aniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-(trifluoromethyl)aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-iodo-6-(trifluoromethyl)aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-(trifluoromethoxy)aniline, -   2-chloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-(trifluoromethoxy)aniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-(trifluoromethoxy)aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-iodo-6-(trifluoromethoxy)aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-[(trifluoromethyl)sulfanyl]aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-[(trifluoromethyl)sulfinyl]aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-[(trifluoromethyl)sulfonyl]aniline, -   2-chloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-[(trifluoromethyl)-sulfanyl]aniline, -   2-chloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-[(trifluoromethyl)-sulfinyl]aniline, -   2-chloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-[(trifluoromethyl)-sulfonyl]aniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-[(trifluoromethyl)-sulfanyl]aniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-[(trifluoromethyl)-sulfinyl]aniline, -   2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-[(trifluoromethyl)-sulfonyl]aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-iodo-6-[(trifluoromethyl)-sulfanyl]aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-iodo-6-[(trifluoromethyl)-sulfinyl]aniline, -   4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-iodo-4-[(trifluoromethyl)-sulfonyl]aniline, -   2-ethyl-4-(2-ethoxy-1,1,1,3,3,3-hexafluoropropan-2-yl)-6-methylaniline, -   4-[2-(4-chlorophenoxy)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-ethyl-6-methylaniline, -   4-[2-(4-chloro-1H-pyrazol-1-yl)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-ethyl-6-methylaniline, -   4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)-2,6-dimethylaniline, -   2-ethyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)-6-methylaniline, -   2,6-dichloro-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)aniline, -   2,6-dibromo-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)aniline, -   4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)-2,6-diiodoaniline, -   2-ethyl-4-[2-ethoxy-1,1,1,3,3,4,4,4-octafluorobutan-2-yl]-6-methylaniline, -   4-[2-(4-chlorophenoxy)-1,1,1,3,3,4,4,4-octafluorobutan-2-yl]-2-ethyl-6-methylaniline, -   4-[2-(4-chloro-1H-pyrazol-1-yl)-1,1,1,3,3,4,4,4-octafluorobutan-2-yl]-2-ethyl-6-methylaniline, -   2,6-dibromo-4-(trifluoromethoxy)aniline, -   2,6-dibromo-4-[(trifluoromethyl)sulfanyl]aniline, -   2,6-dibromo-4-[(trifluoromethyl)sulfinyl]aniline, -   2,6-dibromo-4-[(trifluoromethyl)sulfonyl]aniline, -   2,6-dibromo-4-[(pentafluoroethyl)sulfanyl]aniline, -   2,6-dibromo-4-[(heptafluoropropyl)sulfanyl]aniline, -   2,6-dibromo-4-[(nonafluorobutyl)sulfanyl]aniline, -   2,6-dimethyl-4-(undecafluorocyclohexyl)aniline -   2-ethyl-6-methyl-4-(undecafluorocyclohexyl)aniline -   2,6-dichloro-4-(undecafluorocyclohexyl)aniline -   2,6-dibromo-4-(undecafluorocyclohexyl)aniline -   2,6-diiodo-4-(undecafluorocyclohexyl)aniline, and the like.

The reaction of Preparation method (a) can be carried out in the presence of an appropriate diluent, and examples thereof to be used include aliphatic hydrocarbons (hexane, cyclohexane, heptane, etc.), halogenated aliphatic hydrocarbons (dichloromethane, chloroform, carbon tetrachloride, dichloroethane, etc.), aromatic hydrocarbons (benezene, toluene, xylene, chlorobenzene, etc.), ethers (diethyl ether, dibutyl ether, dimethoxyethane (DME), tetrahydrofuran, dioxane, etc.), esters (ethyl acetate, ethyl propionate, etc.), acid amides (dimethyl formamide (DMF), dimethyl acetamide (DMA), N-methylpyrrolidone, etc.), nitriles (acetonitrile, propionitrile, etc), dimethyl sulfoxide (DMSO), water, a mixture thereof, and etc.

The reaction of Preparation method (a) can be carried out in the presence of an appropriate base, and examples thereof to be used include alkali metal bases, such as lithium hydride, sodium hydride, potassium hydride, butyllithium, tert-butyllithium, trimethylsilyllithium, lithium hexamethyldisilazide, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, cesium carbonate, tripotassium phosphate, sodium acetate, potassium acetate, sodium methoxide, sodium ethoxide, sodium tert-butoxide, and potassium tert-butoxide and organic bases, such as triethylamine, diisopropylethylamine, tributylamine, N-methylmorpholilne, N,N-dimethylaniline, N,N-diethylaniline, 4-tert-butyl-N,N-dimethylanilne, pyridine, picoline, lutidine, diazabicycloundecene, (1,8-diazabicyclo[5.4.0]undec-7-ene), diazabicyclooctane, imidazole and etc.

Preparation method (a) can be carried out within a substantially wide temperature range. It may be generally carried out at the temperature between about −78° C. and about 200° C., preferably between −10° C. and about 150° C. Said reaction is preferably carried out at normal pressure although it may be carried out under elevated or reduced pressure. The reaction time is 0.1 to 72 hours, preferably 0.1 to 24 hours.

For carrying out Preparation method (a), for example, 1 mole of the compound of formula (II) can be reacted with 1 to 3 moles of the compound of formula (III) using, when L¹ in Formula (II) represents hydroxy, 1 to 3 mole of a condensing agent in a diluent, e.g., DMF, or, when L¹ in Formula (II) represents an appropriate leaving group, in the presence of an appropriate base, e.g., pyridine, thereby to obtain the corresponding compound of Formula (I).

Some of the compounds of Formula (IV) as starting materials for Preparation method (b) include the publicly known compounds disclosed in WO 2005/021488 and WO 2005/073165 and their representative examples are as follows:

-   N-[2,6dimethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-fluoro-3-nitrobenzamide, -   N-[2-ethyl-4-(1,     1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluoro-3-nitrobenzamide,     and the like.

On the other hand, representative examples of the novel compounds encompassed by the compounds of Formula (IV) are as follows:

-   2-chloro-4-fluoro-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]benzamide, -   4-fluoro-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]-2-(trifluoromethyl)benzamide, -   4-fluoro-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]-2-nitrobenzamide, -   N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3,4-difluorobenzamide, -   3-chloro-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluorobenzamide, -   3-bromo-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluorobenzamide, -   N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluoro-3-(trifluoromethyl)benzamide, -   N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluoro-1-naphthamide, -   5-bromo-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]pyridine-2-carboxamide, -   6-chloro-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]-nicotinic     acid amide, -   6-chloro-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-nicotinic     acid amide, and the like.

Novel intermediates among the compounds of Formula (IV) are shown in the following Formulae (V-1) to (V-5):

(wherein X¹³ represents halogen, X¹⁴ represents halogen or C₁₋₄ haloalkyl, X¹⁶ and X¹⁷ each independently represent halogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ haloalkoxy, C₁₋₄ haloalkyl-S—, C₁₋₄ haloalkyl-S(O)— or C₁₋₄ haloalkyl-S(O)₂— and J is as defined above);

(wherein X¹⁵ represents halogen, C₁₋₄ haloalkyl or a nitro group and X¹³, X¹⁶, X¹⁷ and J are as defined above);

(wherein X¹³, X¹⁶, X¹⁷ and J are as defined above);

(wherein X¹³, X¹⁶, X¹⁷ and J are as defined above); and

(wherein X¹³, X¹⁶, X¹⁷ and J are as defined above).

Some of the compounds of Formula (IV) as starting materials for Preparation method (b) can be synthesized according to the methods disclosed in WO 2005/021488 and WO 2005/073165. Specifically, they can be synthesized by reacting the compounds of Formula (VI):

(wherein A¹⁻¹, A¹⁻², A¹⁻³, A¹⁻⁴, A¹⁻⁵, G and L¹ each independently have the same meaning as defined above) with the compounds of Formula (III) described above according to Preparation method (a).

Specific preparation method of compound of Formula (IV) is shown in below:

(wherein, Step 1 is done by following the metod descrived in Preparation method (a), Step 2 is done by following the method descrived in Scheme 1, step 1-1, Step 3 is clorination by using N-chlorosuccinimide (NCS) and Step 4 is done by following the method descrived in JP2008-505120A)

The reaction of Preparation method (b) can be carried out in the presence of an appropriate diluent, and examples thereof to be used are the same as the diluents described for Preparation method (a), and preferably dimethylformamide (DMF), dimethylacetamide (DMA), N-methylpyrrolidone or dimethyl sulfoxide (DMSO).

The reaction of Preparation method (b) can be carried out in the presence of an appropriate base, and examples thereof to be used are the same as the bases described for Preparation method (a), and preferably potassium carbonate.

The reaction of Preparation method (b) can be carried out by using a catalyst such as Pd₂ (dba)₃, Pd₂ (dba)₃CHCl₃, (dba=dibenzylideneacetone), Pd (OAc)₂, CuI, and Cu₂O in the presence of an appropriate base, if necessary. Further, if necessary, phosphine type ligands such as 2,2′-bis(diphenyl-phosphino)-1,1′-binaphthalene (BINAP), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos) and tributylphosphine or amine type ligands such as 8-quinolinol, proline and N,N-dimethylglycine can be used.

Preparation method (b) can be carried out within a substantially wide temperature range. It may be generally carried out at a temperature between about −78° C. and about 200° C., preferably between about −10° C. and about 180° C. Said reaction is preferably carried out at normal pressure, although it may be carried out under elevated or reduced pressure. The reaction time is 0.1 to 72 hours, preferably 0.1 to 24 hours.

For carrying out Preparation method (b), for example, 1 mole of the compound of Formula (IV) can be reacted with 1 to 2 moles of the compound represented by W1-H, W2-H, W3-H, W4-H, W5-H, W6-H, W7-H, W8-H or W9-H in the presence of 1 to 3 moles of a base, for example potassium carbonate, in a diluent, for example dimethylformamide, thereby to obtain the compound of Formula (I) of the present invention. In addition, when the catalyst described above is used, for example, 1 mole of the compound of Formula (IV) can be reacted with 1 to 3 moles of the compound represented by W1-H, W2-H, W3-H, W4-H, W5-H, W6-H, W7-H, W8-H or W9-H in the presence of 1 to 3 moles of a base and a catalytic amount of CuI and proline in a diluent, for example dimethylsulfoxide, thereby to obtain the compound of Formula (I) of the present invention.

When A¹⁻¹, A¹⁻², A¹⁻³, A¹⁻⁴ or A¹⁻⁵, encompassed by the compounds of Formula (I) of the present invention obtained according to Preparation method (b), is C—NO₂, the nitro group can be easily converted to other substituents. Specific examples thereof are described in the following Scheme 1.

(In Scheme 1, conc. HCl aq indicates a concentrated hydrochloride acid aqueous solution, Py indicates pyridine, THF indicates tetrahydrofuran, t-Bu indicates tertiary butyl, and DMF indicates N,N-dimethylformamide. According to step 1-1, the nitro group is reduced to give the amino group. According to step 1-2, the acyl group is introduced to the amino group. According to step 1-3, the amino group can be converted to a diazonium salt through Sandmeyer reaction and then to hydrogen after removal of the diazonium salt.)

The compounds of Formula (I-c1) as starting materials for Preparation method (c), can be synthesized according to various methods. Representative examples thereof are shown in Schemes 2, 3, 3-1 and 4.

(In Scheme 2, hydrazine-H₂O indicates a hydrazine hydrate, EtOH indicates ethanol and Py, THF and DMF are as defined above.)

According to Scheme 2, the benzyl halide derivative is obtained through an acid condensation reaction at step 2-1, which is then reacted with phthalimide potassium salt at step 2-2, and subsequently at step 2-3 the phthalimide residue is removed by hydrazine to give the benzylamino derivative. All the reactions defined above can be carried out according to general methods for synthesizing organic compounds.

(In Scheme 3, DMAP indicates 4-dimethylaminopyridine, (Boc)₂O indicates di(t-butyl) bicarbonate, MeOH indicates methanol and conc. HCl aq and EtOH are as defined above.)

(In Scheme 3-1, PPh indicates triphenylphosphine, (Boc)₂O indicates di(t-butyl)bicarbonate, MeOH indicates methanol and conc. HCl aq and EtOH are as defined above.)

The reaction of step 3-2 in Scheme 3 and 3-1 can be carried out according to the method described in the literature (Tetrahedron Letters, 2000, 41, 3513-3516 or Tetrahedron, 2003, 59, 5417-5423).

The reaction of step 3-4 in Scheme 3-1 can be carried out according to the method described in the literature (Synthetic Communications, 1994, 887-890). Other methods can be carried out according to general methods for synthesizing organic compounds.

In accordance with the methods of step 3-2 and step 3-3 in Scheme 3 and 3, 1,4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-(1H-pyrazol-1-yl)benzamide or 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-(1H-1,2,4-triazolyl-1-yl)benzamide may be obtained by using 4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-(1H-pyrazol-1-yl)benzamide or 4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]-3-(1H-1,2,4-triazolyl-1-yl)benzamide, respectively, as a raw material. Further, 3-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide may be similarly obtained from 3-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide.

(In Scheme 4, (Boc)₂O and MeOH are as defined above.)

The reaction of step 4-2 in Scheme 4 can be carried out in the same manner as step 3-2 in Scheme 3. Other methods can be carried out according to general methods for synthesizing organic compounds.

There are additional methods for synthesizing the compounds of Formula (I-c1) as starting materials for Preparation method (c), and examples include a method in which hexamethylenetetramine is reacted with the benzyl halide derivative of Scheme 2 followed by hydrolysis under an acidic condition to give the benzylamino derivative (Delepine amine synthesis, reference literatures: Bull. Soc. Chim. Fr. 1895, 13, S 352, J. Org. Chem. 1993, 58, 270, J. Org. Chem. 1990, 55, 1796, Org. React. 1954, 8, 197.), a method in which a benzyl alcohol derivative or the benzyl halide derivative is converted into a benzyl azide derivative followed by its reduction to give the benzylamino derivative (reference literatures: Chemical Review, 1988, 88, 297, J. Org. Chem., 1993, 58, 5886) or a method in which the benzyl halide derivative is converted to a benzylnitro derivative via Kornblum nitration followed by reduction to give the benzylamino derivative (reference literatures: Organic Synthesis Collective Volume, 1963, 4, 724, Organic Reactions, 1962, 12, 101), etc.

Representative examples of the compounds of Formula (I-c1) as starting materials for Preparation method (c) are as follows:

-   4-(aminomethyl)-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethyl-phenyl]benzamide, -   4-(aminomethyl)-2-fluoro-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-2-fluoro-benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-2,3-difluorobenz-amide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-2,5-difluorobenz-amide, -   4-(aminomethyl)-2-chloro-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]     benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-fluoro-benzamide, -   4-(aminomethyl)-3-chloro-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]     benzamide, -   4-(aminomethyl)-3-bromo-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]     benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methyl     benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-(trifluoro-methyl)benz     amide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-nitro-benzamide, -   4-(aminomethyl)-N-[2,6-dibromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-phenyl]benzamide, -   4-(aminomethyl)-N-[2,6-dimethyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)-phenyl]benzamide, -   4-(aminomethyl)-3-chloro-N-[2,6-dimethyl-4-(1,1,1,2,3,3,4,4,4-nonafluoro-butan-2-yl)phenyl]-benzamide, -   4-(aminomethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]benzamide, -   4-(aminomethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]-3-fluoro-benzamide, -   4-(aminomethyl)-3-bromo-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nona-fluorobutan-2-yl)phenyl]benz-amide, -   4-(aminomethyl)-N-[2,6-dibromo-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)-phenyl]benzamide, -   4-(aminomethyl)-3-chloro-N-[2-ethyl-6-methyl-4-(undecafluorocyclohexyl)-phenyl]benzamide, -   4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-naphthamide, -   4-(aminomethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]-1-naphthamide, -   4-(aminomethyl)-N-[2-ethyl-6-methyl-4-(undecafluorocyclohexyl)phenyl]-1-naphthamide, -   5-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]pyridine-2-carboxamide, -   5-(aminomethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]pyridine-2-carboxamide, -   5-(aminomethyl)-N-[2-ethyl-6-methyl-4-(undecafluorocyclohexyl)phenyl]-pyridine-2-carboxamide, -   6-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]nicotinamide, -   6-(aminomethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]nicotinamide, -   6-(aminomethyl)-N-[2-ethyl-6-methyl-4-(undecafluorocyclohexyl)phenyl]-nicotinamide, -   4-(1-aminoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benzamide, -   4-(1-aminoethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]benzamide, -   4-(1-aminoethyl)-N-[2-ethyl-6-methyl-4-(undecafluorocyclohexyl)phenyl]-benzamide,     and the like.

Specific examples of novel intermediates shown in Schemes 2 to 3 are as follows:

-   4-(chloromethyl)-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethyl-phenyl]benzamide, -   4-(chloromethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benzamide, -   3-chloro-4-(chloromethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-benzamide, -   3-bromo-4-(chloromethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-benzamide, -   4-(chloromethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]benzamide, -   4-(chloromethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]-3-fluoro-benzamide, -   3-chloro-4-(chloromethyl)-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nona-fluorobutan-2-yl)phenyl]benz-amide, -   4-(chloromethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-naphthamide, -   4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-2,6-dimethyl     phenyl]benzamide, -   4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]benzamide, -   3-chloro-4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide, -   3-bromo-4-[[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide, -   4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]-3-nitrobenzamide, -   4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nona-fluorobutan-2-yl)phenyl]benzamide, -   4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nona-fluorobutan-2-yl)phenyl]-3-fluorobenzamide, -   3-chloro-4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,     4,4-nona fluorobutan-2-yl)phenyl]benzamide, -   4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]-1-naphthamide, -   4-cyano-2-fluoro-N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethyl-phenyl]benzamide, -   4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-benzamide, -   4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-2-fluorobenzamide, -   2-chloro-4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benzamide, -   4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methylbenzamide, -   4-cyano-N-[2-ethyl-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-6-methylphenyl]benzamide, -   2-{4-[(4-cyanobenzoyl)amino]-3-ethyl-5-methylphenyl}1,1,1,3,3,3-hexa-fluoropropan-2-yl-methanesulfonate, -   5-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]pyridine-2carboxamide, -   6-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-nicotinamide,     and the like.

The novel intermediates are shown with Formulae (VII-1) to (VII-6):

wherein X¹⁸ represents halogen, hydroxy, azide or 1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl, X¹⁹ represents hydrogen, halogen or C₁₋₄ alkyl; and X⁹, X¹⁰, X¹⁶, X¹⁷, J and m are as defined above;

wherein X¹, X⁹, X¹⁰, X¹⁶, X¹⁷, J and m are as defined above;

wherein X²⁰ represents hydrogen or C₁₋₄ alkyl, X²¹ represents an oxygen or N—X²², X²² represents hydroxy, C₁₋₄ alkyl or C₁₋₄ alkoxy, and X¹⁶, X¹⁷ and J are as defined above;

wherein X²³ represents hydrogen or C₁₋₄ alkyl, X²⁴ represents hydrogen or halogen and X¹⁶, X″ and J are as defined above;

wherein X¹⁶, X¹⁷ and J are as defined above; and

wherein X¹⁶, X¹⁷ and J are as defined above.

Preparation method (c) can be carried out according to general methods for synthesizing organic compounds. In addition, a diluent, a base and the like are the same as those described for Preparation method (a).

With respect to Preparation method (d), an exemplary synthetic method including its starting materials is shown in Scheme 5.

In Scheme 5, corresponding acid chloride and aniline are condensed during step 5-1 to give the anilide, which is subsequently reacted with hydroxylamine during step 5-2 to give the hydroxyimino compound, and although the subsequent step 5-3 is a reductive amination, it can be carried out in the same manner as in step 4-2 described above, and after deprotection during step 5-4, step 5-5 which corresponds to Preparation method (d) is carried out. Preparation method (d) can be carried out in the same manner as in Preparation method (c).]

Representative examples of novel intermediates in Scheme 5 are as follows: N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxamide, N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]-5-(hydroxyimino)-5,6,7,8-tetrahydronaph-thalene-2-carboxamide, and the like.

The novel intermediates described above are summarized in Formula (VIII):

wherein A¹ to A³, B¹ to B⁵, G, Q, X¹⁶ and X²¹ are as defined above.

With respect to Preparation method (e), an exemplary synthetic method including its starting materials is shown in Scheme 6.

Each step in Scheme 6 can be carried out in the same manner as each step in Scheme 5.

Representative examples of novel intermediates in Scheme 6 are as follows:

-   N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-oxoindane-5-carboxamide, -   N-[2ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-(hydroxyimino)indane-5-carboxamide,     and the like.

The novel intermediates defined above are summarized in Formula (IX):

wherein A¹ to A³, B¹ to B⁵, G, Q, X¹⁶ and X²¹ are as defined above.

The compounds of Formula (r-3) as starting materials for Preparation method (f) are publicly known and representative examples thereof include methyl iodide, ethyl iodide, benzyl bromide, dimethyl sulfate, diethyl sulfate, and the like.

The reaction of Preparation method (f) can be carried out in the presence of an appropriate diluent, and examples thereof to be used are the same as the diluents described for Preparation method (a), and preferably DMF.

The reaction of Preparation method (f) can be carried out in the presence of an appropriate base, and examples thereof to be used are the same as the bases described for Preparation method (a), and preferably sodium hydride.

The temperature range, pressure and time for the reaction of Preparation method (f) are the same as those described for Preparation method (a).

For carrying out Preparation method (f), for example, 1 mole of the compound of Formula (I-f1) can be reacted with 1 to 3 moles of the compound of Formula (r-3), for example methyl iodide, in the presence of an appropriate base, for example sodium hydride, in an appropriate diluent, for example DMF, thereby to obtain the compound of Formula (I) of the present invention.

The compounds of Formula (I-g1) as starting materials for Preparation method (g), are encompassed by the compounds of Formula (I) of the present invention and their representative examples are as follows:

-   N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide, -   N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)-benzamide,     and the like.

Examples of the sulfurizing agents to be used in Preparation method (g) are phosphorous pentasulfide, Lawesson reagent and the like.

The reaction of Preparation method (g) can be carried out in the presence of an appropriate diluent, and examples thereof to be used are the same as the diluents described for Preparation method (a), and preferably toluene.

The reaction of Preparation method (g) can be carried out with the reaction temperature, pressure and time that are the same as those for Preparation method (a).

For carrying out Preparation method (g), for example, 1 mole of the compound of Formula (I-g1) can be reacted with 0.5 mole to 3 moles of Lawesson reagent in an appropriate diluent, for example toluene, thereby to obtain the compound of Formula (I).

The compounds of Formula (I) of the present invention exhibit a potent pesticidal effect. Therefore, the compounds of Formula (I) of the present invention can be used as pesticides. The active compounds of Formula (I) of the present invention also exhibit suitable controlling effect against noxious pests without phytotoxicity to cultivated crop plants. In addition, the compounds of the present invention can be used for controlling a wide variety of pests, such as harmful sucking insects, chewing insects and other plant parasitic pests, stored grain pests, hygienic pests etc., and can be applied for the disinfection and destruction of them.

Such harmful insects may be illustrated by examples as follows:

As an insect,

-   -   beetles (Coleopteran), such as adzuki bean beetle         (Callosobruchus Chinensis), maize weevil (Sitophilus zeamais),         red flour beetle (Tribolium Castaneum), large         twenty-eight-spotted lady bird (Epilachna vigintioctomaculata),         barley wireworm (Agriotes ogurae fuscicollis), soy bean beetle         (Anomala rufocuprea), Colorado potato beetle (Leptinotarsa         decemlineata), corn root worm (Diabrotica spp.), Japanese pine         sawyer beetle (Monochamus alternatus endai), rice water weevil         (Lissorhoptrus oryzophilus), powder-post beetle (Lyctus         bruneus);     -   lepidopteran pests, such as gypsy moth (Lymantria dispar),         Lackey moth (Malacosoma neustria), small white (Pieris rapae         crucivora), cotton leafworm (Spodoptera litura), cabbage moth         (Mamestra brassicae), rice stem borer (Chilo suppressalis),         European corn borer (Ostrinia nubilalis), dried currant moth         (Cadra cautella), chyanokokakumonhamaki (Adoxophyes honmai),         codling moth (Cydia pomonella), Turnip Moth (Agrotis segetum),         Wax Moth (Galleria mellonella), Diamondback moth (Plutella         xylostella), tobacco budworm moth (Heliothis virescens), citrus         leaf miner (Phyllocnistis citrella);     -   hemipterous pests, such as green rice leafhopper (Nephotettix         cincticeps), brown planthopper (Nilaparvata lugens), comstock         mealybug (Pseudococcus comstocki), arrowheat scale (Unaspis         yanonensis), Momoaka-aburamusi (Myzus persicas), green apple         aphid (Aphis pomi), cotton aphid (Aphis gossypii), turnip aphid         (Lipaphis erysimi), Nashi-gunbai (Stephanitis nashi), Nezara         (Nezara spp.), greenhouse whitefly (Trialeurodes vaporariorum),         Pshylla (Pshylla spp.);     -   thysanoptera pests, such as palm thrips (Thrips palmi), western         flower thrips (Franklinella occidentalis);     -   orthopteran pests, such as mole cricket (Gryllotalpa Africana),         migratory locust (Locusta migratoria);     -   blattarian pests, such as German cockroach (Blatella germanica),         American cockroach (Periplaneta americana), yamato white ant         (Reticulitermes speratus), Formosan subterranean termite         (Coptotermes formosanus);     -   dipterous pests, such as housefly (Musca domestica), yellow         fever mosquito (Aedes aegypti), Seedcorn maggot (Delia platura),         Aka-ie-ka (Culex pipiens pallens), Sina-hamadara-ka (Anopheles         sinensis), kodaka-aka-ie-ka (Culex tritaeniorhynchus),         serpentine leafininer (Liriomyza trifolii) and the like.

Further, as mites, Carmine spider mite (Tetranychus cinnabarinus), two-spotted spider mite (Tetrahychus urticae), Citrus red mite (Panonychus citri), Pink citrus rust mite (Aculops pelekassi), Tarsonemus (Tarsonemus spp.) and the like can be mentioned.

In addition, as nematodes, sweet potato root-knot nematode (Meloidogyne incognita), pine wood nematode (Bursaphelenchus xylophilus), rice white-tip nematode (Aphelenchoides besseyi), soybean cyst nematode (Heterodera glycines), meadow nematode (Pratylenchus spp.) and the like can be mentioned.

In veterinary medicine field, i.e., veterinary science, the active compounds of the present invention can be effectively used against various harmful animal parasites, particularly, endoparasites and ectoparasites. The term “endoparasites” include in particular worms (tapeworm, eelworm, trematode and the like) and plasmodium (coccidium and the like). The term “ectoparasites” include in general and preferably an arthropod, in particular insects (fly (a fly which can sting and suck), larva of parasitic fly, sucking lice, crab lice, bird lice, flea and the like) or acaroid mites (ticks and the like, for example, hard tick and soft tick) or mites (itch mite, chigger mite, bird mite and the like).

These parasites are as follows:

-   -   from Anoplurida, for example, Haematopinus spp., Linognathus         spp., Pediculus spp., Phtirus spp., Solenopotes spp.;         particularly, for representative examples, Linognathus setosus,         Linognathus vituli, Linognathus ovillus, Linognathus oviformis,         Linognathus pedalis, Linognathus stenopsis, Haematopinus asini         macrocephalus, Haematopinus eurysternus, Haematopinus suis,         Pediculus humanus capitis, Pediculus humanus corporis, Phylloera         vastatrix, Phthirus pubis, Solenopotes capillatus;     -   from Mallophagida, Amblycerina, and Ischnocerina, for example,         Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp.,         Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes         spp., Felicola spp.; particularly, for representative examples,         Bovicola bovis, Bovicola ovis, Bovicola limbata, Damalina bovis,         Trichodectes canis, Felicola subrostratus, Bovicola caprae,         Lepikentron ovis, Werneckiella equi;     -   from Diptera, Nematocerina, and Brachycerina, for example, Aedes         spp., Anopheles ssp., Culex spp., Simulium spp., Eusimulium         spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp.,         Chrysops spp., Odagmia spp., Wilhelmia spp., Hybomitra spp.,         Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp.,         Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp.,         Haematobia spp., Morellia spp., Fannia spp., Glossina spp.,         Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia         spp., Sarcophaga spp., Oestrus spp., Hypoderma spp.,         Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus         spp., Rhinoestrus spp., Tipula spp.; particularly, for         representative examples, Aedes aegypti, Aedes albopictus, Aedes         taeniorhynchus, Anopheles gambiae, Anopheles maculipennis,         Calliphora erythrocephala, Chrysozona pluvialis, Culex         quinquefasciatus, Culex pipiens, Culex tarsalis, Fannia         canicularis, Sarcophaga carnaria, Stomoxys calcitrans, Tipula         paludosa, Lucilia cuprina, Lucilia sericata, Simulium reptans,         Phlebotomus papatasi, Phlebotomus longipalpis, Odagmia ornata,         Wilhelmia equina, Boophthora erythrocephala, Tabanus bromius,         Tabanus spodopterus, Tabanus atratus, Tabanus sudeticus,         Hybomitra ciurea, Chrysops caecutiens, Chrysops relictus,         Haematopota pluvialis, Haematopota italica, Musca autumnalis,         Musca domestica, Haematobia irritans irritans, Haematobia         irritans exigua, Haematobia stimulans, Hydrotaea irritans,         Hydrotaea albipuncta, Chrysomya chloropyga, Chrysomya bezziana,         Oestrus ovis, Hypoderma bovis, Hypoderma lineatum,         Przhevalskiana silenus, Dermatobia hominis, Melophagus ovinus,         Lipoptena capreoli, Lipoptena cervi, Hippobosca variegata,         Hippobosca equina, Gasterophilus intestinalis, Gasterophilus         haemorroidalis, Gasterophilus interrnis, Gasterophilus nasalis,         Gasterophilus nigricornis, Gasterophilus pecorum, Braula coeca;     -   from Siphonapterida, for example, Pulex spp., Ctenocephalides         spp., Tunga spp., Xenopsylla spp., Ceratophyllus spp.;         particularly, for representative examples, Ctenocephalides         canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans,         Xenopsylla cheopis;     -   from Heteropterida, for example, Cimex spp., Triatoma spp.,         Rhodnius spp., Panstrongylus spp.;     -   from Blattarida, for example, Blatta orientalis, Periplaneta         americana, Blattela germanica, Supella spp. (for example,         Suppella longipalpa);     -   from Acari(Acarina), Metastigmata, and Mesostigmata, for         example, Argas spp., Ornithodorus spp., Otobius spp., Ixodes         spp., Amblyomma spp., Rhipicephalus(Boophilus) spp., Dermacentor         spp., Haemophysalis spp., Hyalomma spp., Dermanyssus spp.,         Rhipicephalus spp. (original genus of heteroxenous mites),         Ornithonyssus spp., Pneumonyssus spp., Raillietia spp.,         Pneumonyssus spp., Sternostoma spp., Varroa spp., Acarapis         spp.); particularly, for representative examples, Argas         persicus, Argas reflexus, Ornithodorus moubata, Otobius megnini,         Rhipicephalus(Boophilus) microplus, Rhipicephalus(Boophilus)         decoloratus, Rhipicephalus(Boophilus) annulatus,         Rhipicephalus(Boophilus) calceratus, Hyalomma anatolicum,         Hyalomma aegypticum, Hyalomma marginatum, Hyalomma transiens,         Rhipicephalus evertsi, Ixodes ricinus, Ixodes hexagonus, Ixodes         canisuga, Ixodes pilosus, Ixodes rubicundus, Ixodes scapularis,         Ixodes holocyclus, Haemaphysalis concinna, Haemaphysalis         punctata, Haemaphysalis cinnabarina, Haemaphysalis otophila,         Haemaphysalis leachi, Haemaphysalis longicorni, Dermacentor         marginatus, Dermacentor reticulatus, Dermacentor pictus,         Dermacentor albipictus, Dermacentor andersoni, Dermacentor         variabilis, Hyalomma mauritanicum, Rhipicephalus sanguineus,         Rhipicephalus bursa, Rhipicephalus appendiculatus, Rhipicephalus         capensis, Rhipicephalus turanicus, Rhipicephalus zambeziensis,         Amblyomma americanum, Amblyomma variegatum, Amblyomma maculatum,         Amblyomma hebraeum, Amblyomma cajennense, Dermanyssus gallinae,         Ornithonyssus bursa, Ornithonyssus sylviarum, Varroa jacobsconi;     -   from Actinedida(Prostigmata), and Acaridida(Astigmata), for         example, Acarapis spp., Cheyletiella spp., Ornithocheyletia         spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula         spp., Listrophorus spp., Acarus spp., Tyrophagus spp.,         Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes         spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres         spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.;         particularly, Cheyletiella yasguri, Cheyletiella blakei, Demodex         canis, Demodex bovis, Demodex ovis, Demodex caprae, Demodex         equi, Demodex caballi, Demodex suis, Neotrombicula autumnalis,         Neotrombicula desaleli, Neoschonegastia xerothermobia,         Trombicula akamushi, Otodectes cynotis, Notoedres cati,         Sarcoptis canis, Sarcoptes bovis, Sarcoptes ovis, Sarcoptes         rupicaprae(=S. caprae), Sarcoptes equi, Sarcoptes suis,         Psoroptes ovis, Psoroptes cuniculi, Psoroptes equi, Chorioptes         bovis, Psoergates ovis, Pneumonyssoidic mange, Pneumonyssoides         caninum, Acarapis woodi.

The active compounds of the present invention are also useful for controlling an arthropod, a worm and a plasmodium which attacks an animal. Examples of the animal include an agricultural animals such as a cow, a sheep, a goat, a horse, a pig, a donkey, a camel, a buffalo, a rabbit, a chicken, a turkey, a duck, a goose, a nursery fish, a honey bee, etc. In addition, a pet which is also called as a companion animal, for example, a dog, a cat, a caged bird, an aquarium fish, and an animal for experimental testing (e.g., a hamster, a guinea pig, a rat, a mouse and the like) is also included.

With control of the arthropod, worm and/or plasmodium by using the active compounds of the present invention, death ratio of a host animal can be reduced and productivity (for meat, milk, wool, leather, egg, and honey) and health of the animal can be improved. As a result, it is intended to achieve economically more favorable and simple animal breeding.

For example, it is preferable that introduction of blood from a parasite to a host is ether prevented or inhibited (if possible). Parasite control can be useful for preventing infection which is caused by inflammatory pathogens.

The term “control” that is used in the present specification regarding a veterinary medicine field means that the active compounds are effective for reducing the occurrence ratio of each parasite in an animal infected with it to an innoxious level. More specifically, the term “to control” means that the active compounds of the present invention are effective for destroying parasites, inhibiting growth or propagation thereof.

In the present invention, substances having pesticidal effects against harmful pests including all of such pests are referred to as pesticides.

When used as pesticides, the active compounds of the present invention can be prepared in a form of a common preparation. Such preparation form may includes, for example, liquids, emulsions, wettable powders, granulated wettable powders, suspensions, powders, foams, pastes, tablets, granules, aerosols, natural or synthetic agents impregnated with the active compounds, microcapsules, coating agents for seeds, formulations equipped with a combustion device (the combustion device can be a smoke or fog cartridge, a can or a coil, etc.) and ULV (cold mist, warm mist), and the like.

These formulations can be produced by known methods per se. For example, they can be prepared by mixing the active compounds with extenders, namely, liquid diluents or carriers; liquefied gas diluents or carriers; solid diluents or carriers and, optionally, with surfactants, namely, emulsifiers and/or dispersants and/or foam formers and the like.

In case of using water as an extender, for example, organic solvents can be used as auxiliary solvents.

The liquid diluents or carriers may include, for example, aromatic hydrocarbons (e.g. xylene, toluene, alkylnaphthalene etc.), chlorinated aromatic or chlorinated aliphatic hydrocarbons (e.g. chlorobenzenes, ethylene chlorides, methylene chlorides etc.), aliphatic hydrocarbons (e.g. cyclohexanes or paraffins (e.g. mineral oil fractions)), alcohols (e.g. butanol, glycol and ethers or esters thereof, etc.), ketones (e.g. acetone, methylethylketone, methylisobutylketone, cyclohexanone etc.), strong polar solvents (e.g. dimethylformamide, dimethylsulfoxide etc.), water and the like.

The liquefied gas diluent or carrier may include those present as gas at atmospheric pressure and temperature, for example, bulan, propane, nitrogen gas, carbon dioxide, and aerosol propellant such as halogenated hydrocarbons.

Examples of the solid diluents may include ground natural minerals (for example, kaolins, clay, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, etc.) and ground synthetic minerals (for example, highly dispersed silicic acid, alumina and silicate, etc.) and the like.

Examples of the solid carriers for granules may include crushed and fractionated rocks (for example, calcite, marble, pumice, sepiolite and dolomite, etc.), synthetic granules of inorganic or organic powders, and fine granules of organic materials (for example, sawdust, coconut shells, maize cobs and tobacco stalks, etc.) and the like.

Examples of the emulsifiers and/or foam formers may include nonionic and anionic emulsifiers [for example, polyoxyethylene fatty acid esters, polyoxyethylene fatty acid alcohol ethers (for example, alkylaryl polyglycol ether), alkyl sulfonates, alkyl sulfates and aryl sulfonates] and albumin hydrolysates and the like.

The dispersants include lignin sulfite waste liquor and methylcellulose.

Binders may also be used in formulations (powders, granules and emulsion). Examples of the binders may include carboxymethyl cellulose, natural or synthetic polymers (for example, gum arabic, polyvinyl alcohol and polyvinyl acetate, etc.).

Colorants may also be used. Examples of the colorants may include inorganic pigments (for example, iron oxide, titanium oxide and Prussian blue, etc.), organic dyes such as Alizarin dyes, azo dyes or metal phthalocyanine dyes, and further, trace elements such as salts of iron, manganese, boron, copper, cobalt, molybdenum or zinc.

The formulation may include the above active component in an amount of 0.1 to 95 wt %, preferably 0.5 to 90 wt %.

The active compounds of Formula (I) of the present invention can be provided as a mixture with other active compounds such as a pesticide, a poison bait, a sterilizing agent, an acaricidal agent, a nematocide, a fungicide, a growth regulating agent, a herbicide, and the like in a form of commercially useful formulation or an application form prepared from formulation thereof. The pesticide may include, for example, an organic phosphorous agent, carbamate agent, carboxylate agent, chlorinated hydrocarbon agent, and pesticidal substance produced by microorganisms, etc.

Further, the active compounds of Formula (I) of the present invention can be provided as a mixture with a synergist. Such formulation and application form may include those that are commercially useful. The synergist is not necessarily active by itself. Rather, it is the compound which enhances the activity of the active compounds.

The amount of the active compounds of Formula (I) of the present invention that is included in a commercially useful form may vary over a broad range.

The concentration of the active compounds of Formula (I) of the present invention for actual use can be, for example, between 0.0000001 and 100% by weight, preferably between 0.00001 and 1% by weight.

The compounds of Formula (I) of the present invention can be used according to any common method that is appropriate for an application form.

The active compounds of the present invention have stability that is effective for alkaline substances present in lime materials when the compounds are used against hygienic pests and storage pests. In addition, it exhibits excellent residual effectiveness in woods and soils.

Generally, when the active compounds of the present invention are used for the treatment of animals, they can be directly applied to the animal. Preferably, the compounds are applied in a form of pharmaceutical composition which may include a vehicle, an auxiliary agent, or both, that are known in the field and pharmaceutically acceptable.

For a veterinary medicine field and animal breeding, the active compounds can be applied (administered) according to various known ways, for example; intraintestinal administration with a tablet, a capsule, a drink, a drinkable medicine, granules, paste, and bolus administration, feed-through method, suppository; non-intraintestinal administration based on skin application such as injection (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.), embedding, intranasal application including bathing or immersion, spray, pouring, dropping, washing and scattering, and by using a molding article containing the active compounds such as a necklace, an earmark, a tag, a leg brace, a net, a marking device and the like. The active compounds of the present invention can be formulated into an appropriate formulation form that can be applied with a shampoo, aerosol, a non-pressurized spray, for example a pump spray and a vaporizer spray, etc.

When used for livestock, fouls, pets and the like, the active compounds of the present invention can be used as a formulation which includes them in an amount of 1 to 80 wt % (for example, powders, wettable powders (WP), emulsion, emulsifiable concentrate (EC), fluid, homogeneous solution and suspension concentrate (SC)), and Formulation can be applied as it is or after dilution (for example, dilution of 100 to 10,000 times), or as a chemical shower as an alternative method.

When used in a veterinary medicine field, the active compounds of the present invention can be used in combination with other appropriate synergistic agent or other active compounds, for example an acaricide, an insecticide, a parasticide, an anti plasmodium agent, etc.

The active compounds of the present invention have low toxicity and can be safely used for warm-blooded animals.

Herein below, the present invention is described in greater detail with reference to the following examples. However, it is evident that the present invention is not limited thereto alone.

EXAMPLES Synthetic Example 1 Synthesis of N-[2,6-d]bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 1-78).

Step 1-1: Synthesis of 4-(1H-1,2,4-triazol-1-yl)benzoyl Chloride

4-(1H-1,2,4-triazol-1-yObenzoic acid (0.90 g) was suspended in toluene. To the suspension, thionyl chloride (5.7 g) and an catalytic amount of N,N-dimethylformamide (2 to 3 drops) were added and the mixture was refluxed under heating for 4 hours. After adjusting the reaction solution to room temperature, the solvent was distilled off under reduced pressure to obtain 4-(1H-1,2,4-triazol-1-yl)-benzoyl chloride as a crude product (0.95 g). Without further purification, the crude product was used for the next reaction.

Step 1-2: Synthesis of N-[2,6-dibromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-phenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 1-78)

2,6-Dibromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)aniline (0.45 g) was dissolved in pyridine (5 ml). To the solution, the crude product of 4-(1H-1,2,4-triazol-1-yl)benzoyl chloride (0.45 g) was added and the mixture was refluxed under heating for 1.5 hours. After cooling to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with 2N hydrochloric acid and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a residue, which were then dissolved in tetrahydrofuran (20 ml), added with a 2N sodium hydroxide solution (5 ml) and stirred under heating at 50° C. for 2 hours. After cooling to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by column chromatography to obtain N-[2,6-d]bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (0.18 g, yield 28%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 2 Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]-3-nitro-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 1-39).

N-[2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluoro-3-nitrobenzamide (1.5 g, see WO 2005/073165) and 1H-1,2,4-triazole (0.24 g) were dissolved in N,N-dimethylformamide (15 ml). To the solution, potassium carbonate (0.88 g) was added and the mixture was stirred under heating at 70° C. for 3 hours. After cooling to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The resulting crude product was purified by column chromatography to obtain N-[2ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-nitro-4-(1H-1,2,4-triazol-1-yl)benzamide (1.4 g, yield 80%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 3 Synthesis of 3-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 1-38).

N-[2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-nitro-4-(1H-1,2,4-triazol-1-yl)benzamide (1.3 g) was dissolved in ethanol (20 ml). To the solution, tin (II) chloride dihydrate (1.4 g) and conc. hydrochloric acid (1 ml) were added and the mixture was stirred under heating at 60° C. for 4 hours. The reaction solution was neutralized with potassium carbonate while it is vigorously stirred with addition of ethyl acetate and water. The resulting precipitates were filtered using Celite, the aqueous phase was separated from the organic phase and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with brine and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by column chromatography to obtain 3-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (1.0 g, yield 97%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 4 Synthesis of Methyl[5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]carbamoyl}-2-(1H-1,2,4-triazol-1-yl)phenyl]carbamate (Compound No. 1-47).

3-Amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (0.2 g) and pyridine (0.05 g) were dissolved in tetrahydrofuran (5 ml). To the solution, ethyl chlorocarbonate (0.04 g) was added under ice cooling. After adjusting to room temperature, the mixture was stirred for 1 hr. The reaction mixture was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by column chromatography to obtain methyl[5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]carbamoyl}-2-(1H-1,2,4-triazol-1-yl)phenyl]carbamate (0.14 g, yield 58%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 5 Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 1-31).

N,N-dimethylformamide (3 ml) was heated to 65° C. and added with tert-butyl nitrite (0.15 g). To the solution, an N,N-dimethylformamide solution (2 ml) in which 3-amino-N-[2-ethyl-4-(1,1,1,2,3, 3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl) benzamide (0.5 g) has been dissolved was slowly added dropwise, while maintaining the temperature of 65° C. After confirming that no more gas is generated, the mixture was adjusted to room temperature and added with a mixture including 2N hydrochloric acid and a small amount of ice. The mixture was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with 2N hydrochloric acid, and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by column chromatography to obtain N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (0.31 g, yield 61%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 6 Synthesis of 4-(acetamidomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]benzamide (Compound No. 5-28).

Step 6-1: Synthesis of 4-(chloromethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide (Compound No. F-3)

2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline (0.50 g) and pyridine (0.20 g) were dissolved in tetrahydrofuran (10 ml). To the solution, 4-(chloromethyl)benzoyl chloride (0.33 g) and 4-dimethylaminopyridine (0.02 g) were added and the mixture was refluxed under heating for 3 hours. After adjusting to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with 2N hydrochloric acid and dried over Mg(SO₄). After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was washed with hexane to obtain 4-(chloro methyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]benzamide (0.62 g, yield 74%).

¹H-NMR (CDCl₃): see the Table below.

Step 6-2: Synthesis of 4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide (Compound No. F-4)

4-(Chloromethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benz amide (1.2 g) was dissolved in N,N-dimethylformamide (15 ml). To the solution, potassium phthalimide (0.95 g) and potassium iodide (0.09 g) were added and the mixture was stirred under heating at 60° C. for 2 hours. After adjusting to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was washed with tert-butyl methyl ether to obtain 4-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]-benzamide (0.85 g, yield 56%).

¹H-NMR (CDCl₃): see the Table below.

Step 6-3: Synthesis of 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6methylphenyl]benzamide (Compound No. 5-27)

4-[(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]benzamide (0.80 g) was dissolved in ethanol (20 ml). To the solution, hydrazine monohydrate (0.28 g) was added and the mixture was stirred under heating at 60° C. for 4 hours. After adjusting to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate solution and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl] benzamide as a crude product (0.63 g). Without further purification, the crude product was used for the next reaction.

¹H-NMR (CDCl₃): see the Table below.

Step 6-4: Synthesis of 4-(acetamidomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide (Compound No. 5-28)

The crude product of 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]benzamide (0.30 g) was dissolved in tetrahydrofuran (5 ml). To the solution, acetic anhydride (0.07 g) was added and the mixture was stirred at room temperature for 2 hours. The reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with 2N hydrochloric acid and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was separated and purified by column chromatography to obtain 4-(acetamidomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]benzamide (0.27 g, yield 77%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 7 Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]-3-{[(3,3,3-trifluoropropanoyl)amino]methyl}benzamide (Compound No. 5-102).

Step 7-1: Synthesis of 4-cyano-3-methylbenzoic Acid

4-Bromo-3-methylbenzoic acid (3.0 g) was dissolved in N,N-dimethylformamide (20 ml). The resulting solution was subjected to deaeration three times under argon atmosphere (i.e., the reaction solution was de-pressurized to 20 mmHg, and then brought back to atmospheric pressure under argon atmosphere). To the solution, zinc cyanide (1.6 g) and tetrakis(triphenylphosphine) palladium (0) (1.6 g) were added and the mixture was stirred under heating at 90° C. for 6 hours under argon atmosphere. After adjusting to room temperature, precipitates were filtered off. The filtrate was diluted with water, added with lithium hydroxide monohydrate (2.9 g) and washed twice with tert-butyl methyl ether. The aqueous phase was acidified with 2N hydrochloric acid and extracted twice with ethyl acetate. The organic phases were combined, washed with brine and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain 4-cyano-3methylbenzoic acid as a crude product (1.9 g). Without further purification, the crude product was used for the next reaction.

Step 7-2: Synthesis of 4-cyano-3-methylbenzoyl Chloride

The crude product of 4-cyano-3-methylbenzoic acid (1.0 g) was suspended in dichloromethane. To the mixture, oxalyl chloride (1.2 g) and an catalytic amount of N,N-dimethylformamide (2 to 3 drops) were added under ice cooling. After adjusting to room temperature, the reaction solution was stirred for three hours. The solvent was distilled off under reduced pressure to obtain 4-cyano-3-methylbenzoyl chloride as a crude product (1.0 g).

Step 7-3: Synthesis of 4-cyano-N[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methylbenzamide (Compound No. I-5)

2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline (1.7 g) and pyridine (0.88 g) were dissolved in tetrahydrofuran (30 ml). To the solution, the crude product of 4-cyano-3-methylbenzoyl chloride (1.0 g) and 4-dimethylaminopyridine (0.03 g) were added and the mixture was stirred under heating at 50° C. for 2 hours. After adjusting to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with 2N hydrochloric acid and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was washed with a mixed solvent of hexane and ethyl acetate (ethyl acetate 10%) to obtain 4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methylbenzamide (2.1 g, yield 83%).

¹H-NMR (CDCl₃): see the Table below.

Step 7-4: Synthesis of Tert-butyl (4-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]carbamoyl}-2-methylbenzyl)carbamate (Compound No. 5-104)

4-Cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methylbenz amide (2.0 g) was dissolved in methanol (50 ml). To the solution, di-tert-butyl bicarbonate (2.0 g) and nickel (II) chloride hexahydrate (0.53 g) were added and dissolved therein. To the reaction solution, NaBH₄ (0.80 g) was slowly added under ice cooling. Upon the completion of the reaction, diethylenetriamine (4.9 ml) was added, and then stirred for 30 minutes while adjusting the mixture to room temperature. The mixture was diluted with ethyl acetate and water and vigorously stirred for 5 minutes. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by column chromatography to obtain tert-butyl (4-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]carbamoyl}-2-methylbenzyl)carbamate (1.8 g, yield 72%).

¹H-NMR (CDCl₃): see the Table below.

Step 7-5: Synthesis of 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6methylphenyl]-3-methylbenzamide (Compound No. 5-98).

Tert-Butyl (4-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-carbamoyl}-2-methylbenzyl)carbamate (1.7 g) was dissolved in ethanol (30 ml). To the solution, conc. hydrochloric acid (3 ml) was added and the mixture was stirred under heating at 60° C. for 4 hours. After adjusting to room temperature, the reaction solution was diluted with ethyl acetate and water and neutralized with sodium hydrocarbonate under vigorous stirring. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with water and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methyl benzamide as a crude product (0.81 g). Without further purification, the crude product was used for the next reaction.

¹H-NMR (CDCl₃): see the Table below.

Step 7-6: Synthesis of N-[2-ethyl-4(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-{[(3,3,3-trifluoropropanoyl)amino]methyl}benzamide (Compound No. 5-102)

To a methylene chloride solution (2 ml) of the crude product of 4-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-methylbenzamide (150 mg) and 3,3,3-trifluoropropionic acid (50 mg), 1-ethyl-3-(3-dimethyl-aminopropyl)carbodiimide hydrochloride (93 mg) was added under stirring at room temperature. The mixture was further stirred for 3 hours. The reaction solution was separated and purified by column chromatography to obtain N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-{[(3,3,3-trifluoropropanoyl)amino]methyl}benzamide (155 mg, yield 85%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 8 Synthesis of 4-(1-acetamidoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]benzamide (Compound No. 9-2)

Step 8-1: Synthesis of 4-acetyl-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]benzamide (Compound No. H-1)

4-Acetylbenzoic acid (3.5 g) was suspended in methylene chloride (30 ml). To the suspension, oxalyl chloride (1.5 g) and a small amount of N,N-dimethylformamide (2 to 3 drops) were added and the mixture was stirred at room temperature for 2 hours. After the reflux under heating for 30 minutes, the solvent and oxalyl chloride were distilled off under reduced pressure. To the residue, 2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline (1.5 g) dissolved in pyridine (30 ml) was added and the reaction solution was stirred at 140° C. for 4 hours. After adjusting to the room temperature, the reaction solution was added with a 1N hydrochloric acid aqueous solution and extracted twice with ethyl acetate. The organic phases were combined, washed with a 1N hydrochloric acid solution and water in turns and dried over anhydrous magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure. The residue was purified by column chromatography to obtain 4-acetyl-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl] benzamide (2.4 g, yield 47%).

¹H-NMR (CDCl₃): see the Table below.

Step 8-2: Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-[N-hydroxyethaneimidoyl]benzamide (Compound No. H-2)

4-Acetyl-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-benzamide (2.2 g) was dissolved in ethanol (15 ml) and water (15 ml). To the solution, sodium acetate (0.6 g) and hydroxylamine hydrochloride (0.30 g) were added and the mixture was refluxed under heating for 4 hours. The reaction solution was extracted twice with ethyl acetate. The organic phases were combined, washed with water and dried over anhydrous magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-[N-hydroxyethaneimidoyl]benzamide (2.1 g, yield 96%).

¹H-NMR (CDCl₃): see the Table below.

Step 8-3: Synthesis of tert-butyl [1-(4-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]carbamoyl}-phenyl)ethyl]carbamate (Compound No. 9-7)

N-[2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-[N-hydroxy-ethaneimidoyl]benzamide (2.1 g) was dissolved in methanol (25 ml) and 1,4-dioxane (5 ml). To the solution, di-tert-butyl bicarbonate (1.8 g) and nickel (II) chloride hexahydrate (0.49 g) were added. The resulting solution was cooled to 4° C., and sodium borohydride (0.62 g) was added in small portions. The mixture was stirred at 4° C. for 2 hours. Then, diethylenetriamine (1.1 g) was added and stirred for 30 minutes, and then diluted the solution with water followed by extraction twice with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution and water in turns and dried over anhydrous magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure. The residue was purified by column chromatography to obtain tert-butyl [1-(4-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]carbamoyl}-phenyl)ethyl]carbamate (1.7 g, yield 62%).

¹H-NMR (CDCl₃): see the Table below.

Step 8-4: Synthesis of 4-(1-aminoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide (Compound No. 9-1)

Tert-Butyl [1-(4-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]carbamoyl}phenyl)ethyl]carbamate (1.7 g) was dissolved in methylene chloride (20 ml). To the solution, trifluoroacetic acid (1.5 g) was added and the mixture was stirred at room temperature for 3 hours. The solvent was distilled off under reduced pressure and the residue was neutralized by adding water and potassium carbonate followed by extraction twice with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution and water in turns and dried over anhydrous magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain 4-(1-aminoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benzamide as a crude product (1.8 g).

¹H-NMR (CDCl₃): see the Table below.

Step 8-5: Synthesis of 4-(1-acetamidoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-hepta-fluoropropan-2-yl)-6-methylphenyl]benzamide (Compound No. 9-2)

4-(1-Aminoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]benz amide (0.4 g) was dissolved in methylene chloride (15 ml). To the solution, acetic acid (0.06 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.26 g) and an catalytic amount of dimethylaminopyridine were added and the mixture was stirred at room temperature for 3 hours. The solvent was distilled off under reduced pressure and the residue was added with water followed by extraction twice with ethyl acetate. The organic phases were combined, washed with water and dried over anhydrous magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure. The residue was purified by column chromatography to obtain 4-(1-acetamidoethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]benzamide (0.35 g, yield 95%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 9 Synthesis of 1-acetamide-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]indane-5-carboxamide (Compound No. 10-2).

Step 9-1: Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1xoindane-carboxamide (Compound No. L-1).

1-Oxoindane-5-carboxylic acid (3.0 g) was suspended in methylene chloride (30 ml), and oxalyl chloride (1.8 g) and a small amount of N,N-dimethylformamide (2 to 3 drops) were added thereto, and then stirred at room temperature for 2 hours. Thereafter, the solvent and oxalyl chloride were distilled off under reduced pressure. Pyridine (1.6 g) and 2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline (1.6 g) dissolved in methylene chloride (30 ml) were added to the residue, and the mixture was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure and the residue was purified by column chromatography to obtain N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-oxoindane-5-carboxamide (2.4 g, yield 53%).

¹H-NMR (CDCl₃): see the Table below.

Step 9-2: Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]-1-(hydroxyimino)indane-5-carboxamide (Compound No. L-2).

N-[2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-oxoindane-5-carboxamide (2.4 g) was dissolved in ethanol (40 ml), and sodium acetate (0.85 g) and hydroxylamine hydrochloride (0.43 g) were added thereto, and then stirred and heated at reflux temperature for 2 hours. The reaction solution was brought back to room temperature and diluted with water. The resulting crystals were collected by filtration and dried to obtain N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-(hydroxyimino) indane-5-carboxamide (2.3 g, yield 91%).

¹H-NMR (CDCl₃): see the Table below.

Step 9-3: Synthesis of tert-butyl 5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]carbamoyl}-2,3-dihydro-1H-inden-1-yl)carbamate (Compound No. 10-7).

N-[2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-1-(hydroxyimino)indane-5carboxamide (2.3 g) was dissolved in methanol (40 ml) and 1,4-dioxane (20 ml), and di-tert-butyl bicarbonate (2.1 g) and nickel (II) chloride hexahydrate (0.56 g) were added thereto. The solution was cooled to 4° C., small portions of sodium borohydride (0.45 g) were added thereto, and then stirred at 4° C. for 2 hours. To the mixture, diethylenetriamine (1.2 g) was added and stirred for 30 min. The solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution and water, and then dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography to obtain tert-butyl 5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]carbamoyl}-2,3-dihydro-1H-inden-1-yl)carbamate (2.3 g, yield 87%).

¹H-NMR (CDCl₃): see the Table below.

Step 9-4: Synthesis of 1-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]indane-5-carboxamide

Tert-butyl (5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-carbamoyl}-2,3-dihydro-1H-inden-1-yl)carbamate (1.3 g) was dissolved in methylene chloride (15 ml), trifluoroacetic acid (1.5 g) was added thereto and then stirred at room temperature for 3 hours. The solvent was distilled off under reduced pressure. Water and potassium carbonate were added to neutralize the residue and extracted twice with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution and water sequentially, and then dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain 1-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]indane-5-carboxamide as a crude product (0.84 g). The crude product was used for the next step without further purification.

Step 9-5: Synthesis of 1-acetamide-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]indane-5-carboxamide (Compound No. 10-2).

The crude product of 1-amino-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]indane-5-carboxamide (0.12 g) was dissolved in methylene chloride (2 ml). Acetic anhydride (0.04 ml) was added to the solution and stirred at room temperature for 2 hours. The reaction solution was separated and purified by column chromatography to obtain 1-acetamide-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]indane-5-carboxamide (0.07 g, yield 52%).

¹H-NMR (CDCl₃): see the Table below.

Synthetic Example 10 Synthesis of 4-(acetamidemethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (Compound No. 5-229).

Step 10-1: Synthesis of N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-nitrobenzamide (Compound No. N-1).

4-Nitrobenzoyl chloride (4.55 g) was dissolved in a pyridine (30 ml) solution of 2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)aniline (2.7 g). The solution was refluxed under heating for 3 hours. After cooling to room temperature, the solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined and dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure. The residue was dissolved in tetrahydrofuran (30 ml), and an aqueous solution (5 ml) containing sodium hydroxide (2.0 g) was added, and then stirred at room temperature for 4 hours. The reaction solution was extracted twice with ethyl acetate. The organic phases were combined, washed with 1 N hydrochloric acid and water, and dried over anhydrous magnesium sulfate. The drying agent (i.e., anhydrous magnesium sulfate) was removed by filtration, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography to obtain N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-nitrobenzamide (3.27 g, yield 83.4%).

¹H-NMR (CDCl₃) δ: 7.68 (2H, d), 7.80 (1H, s), 8.13 (2H, d), 8.39 (2H, d).

Step 10-2: Synthesis of 4-amino-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)phenyl]benzamide (Compound No. O-1).

N-[2,6-Dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-nitro-benzamide (3.2 g) and nickel (II) chloride hexahydrate (3.33 g) were dissolved in methanol (30 ml). To the reaction solution, NaBH₄ (0.80 g) was added slowly under ice cooling, and the mixture was stirred for 1 hour while increasing the temperature to room temperature. Aqueous ammonia (about 5 ml) was added to the reaction solution under stirring, and then diluted with ethyl acetate and water. The organic phase was separated and the aqueous layer was extracted with ethyl acetate. The organic phases were combined, and then dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then separated and purified by column chromatography to give 4-amino-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-benzamide (2.89 g, yield 96%).

¹H-NMR (CDCl₃) δ: 6.72 (2H, d), 7.56 (1H, s), 7.63 (2H, s), 7.78 (2H, d).

Step 10-3: Synthesis of 4-amino-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (Compound No. O-4).

To the toluene (30 ml) solution in which 4-amino-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)phenyl]benzamide (2.80 g) is dissolved, N-chlorosuccinimide (0.87 g) was added. The reaction solution was stirred for 6 hours at 80° C. under heating. The solution was cooled to room temperature, diluted with water and extracted twice with ethyl acetate. The organic phases were combined, and then dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then separated and purified by column chromatography to give 4-amino-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl] benzamide (2.03 g, yield 67.3%).

¹H-NMR (CDCl₃) δ: 4.53 (2H, s), 6.82 (1H, d), 7.52 (1H, s), 7.64 (2H, s), 7.68 (1H, dd), 7.90 (1H, d).

Step 10-4: Synthesis of 3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)phenyl]-4-iodobenzamide (compound No. A-7).

To the acetonitrile (20 ml) solution in which 4-amino-3-chloro-N-[2,6-di-chloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (1.95 g) and diiodomethane (1.30 ml) are dissolved, an acetonitrile solution (5 ml) containing t-butyl nitrite (1.05 ml) was added dropwise. The solution was stirred for 1 hour at room temperature and then stirred further for 1 hour at 60° C. under heating. The reaction mixture was cooled, diluted with ethyl acetate, and washed twice with water and twice with an aqueous solution of sodium bisulfite. The organic phase was dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then separated and purified by column chromatography to give 3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-iodobenzamide (1.65 g, yield 68.8%).

¹H-NMR (CDCl₃) δ: 7.49 (1H, dd), 7.60 (1H, s), 7.67 (2H, s), 8.00 (1H, d), 8.04 (1H, d).

Step 10-5: Synthesis of 3-chloro-4-cyano-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (Compound No. 1-38).

3-Chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-iodobenzamide (1.59 g) was dissolved in N,N-dimethylformamide (20 ml). The resulting solution was deaerated under argon atmosphere, and then zinc cyanide (0.38 g) and tetrakis(triphenyl phosphine) palladium (0) (0.37 g) were added thereto. The mixture was heated and stirred for 7 hours at 80° C. under argon atmosphere. The reaction mixture was cooled, diluted with ethyl acetate, and then washed twice with water. The organic phase was dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then purified by column chromatography to give 3-chloro-4-cyano-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-phenyl]-benzamide (0.90 g, yield 68.2%).

¹H-NMR (CDCl₃) δ: 7.69 (2H, s), 7.72 (1H, s), 7.85 (1H, d), 7.93 (1H, dd), 8.09 (1H, d).

Step 10-6: Synthesis of tert-butyl (2-chloro-4-{[2,6-dichloro-4-(1,1,1,2,3,3,3heptafluoro propan-2-yl)phenyl]carbamoyl} benzyl)carbamate (Compound No. 5-317).

3-Chloro-4-cyano-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-phenyl]benzamide (0.85 g) was dissolved in methanol (50 ml). To the solution, di-tert-butyl bicarbonate (0.75 g) and nickel (II) chloride hexahydrate (0.41 g) were dissolved. To this reaction solution, NaBH₄ (0.62 g) was added in small portions under stirring and ice cooling conditions. After stirring for 2 hours, diethylenetriamine (3.7 ml) was added to the reaction solution, and then further stirred for 30 min while increasing the temperature to room temperature. The mixture was diluted with ethyl acetate and water, and then vigorously stirred for 5 min. The organic phase was separated and the aqueous layer was extracted with ethyl acetate. The organic phases were combined, washed with a saturated sodium bicarbonate aqueous solution, and then dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then purified by column chromatography to give tert-butyl (2-chloro-4-{[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]carbamoyl}benzyl) carbamate (0.95 g, yield 92.3%).

¹H-NMR (CDCl₃) δ: 1.46 (9H, s), 4.47 (2H, d), 5.09 (1H, s), 7.55 (1H, d), 7.63 (1H, s), 7.67 (2H, s), 7.82 (1H, dd), 7.96 (1H, d).

Step 10-7: Synthesis of 4-(aminomethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (Compound No. 5-228).

Tert-butyl (2-chloro-4-{[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-phenyl]carbamoyl}benzyl)carbamate (0.85 g) was dissolved in methylene chloride (15 ml). Trifluoroacetic acid (2 ml) was added to the solution, and the mixture was stirred at room temperature for 16 hours. The solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride (15 ml), and an aqueous solution of potassium carbonate was added to the solution under stirring. The organic phase was separated and the aqueous layer was extracted with methylene chloride and dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product (0.65 g) of 4-(aminomethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3heptafluoro propan-2-yl)-phenyl]benzamide. The crude product was used for the next step without further purification.

¹H-NMR: see the Table below.

Step 10-8: Synthesis of 4-(acetamidemethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (Compound No. 5-229).

The crude product of 4-(aminomethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (0.15 g) was dissolved in methylene chloride (2 ml). Acetic anhydride (0.05 ml) was added to the solution and stirred for 2 hours at room temperature. The reaction solution was separated and purified by column chromatography to obtain 4-(acetamidemethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide (0.13 g).

¹H-NMR: see the Table below.

Synthetic Example 11 Synthesis of 3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-[(propionylamino)methyl]benzamide (Compound No. 5-230).

To the methylene chloride solution (2 ml) of the crude product of 4-(aminomethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-phenyl]benzamide (150 mg), which had been obtained from Step 10-7 of Synthetic example 10, and propionic acid (23 mg), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (93 mg) was added at room temperature under stirring. The mixture was then stirred for 3 hours. The reaction solution was separated and purified by column chromatography to obtain 3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-[(propionylamino)methyl]benzamide (150 mg).

¹H-NMR: see the Table below.

Synthetic Example 12 Synthesis of 3-(acetamidemethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 12-3).

Step 12-1: Synthesis of 3-cyano-N[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]-4-fluorobenzamide

3-Cyano-4-fluorobenzoic acid (1.0 g) was suspended in toluene (20 ml), thionyl chloride (0.79 g) and a small amount of N,N-dimethylformamide (2 to 3 drops) were added thereto, and the mixture was heated and stirred for 6 hours at reflux temperature. After cooling to room temperature, the solvent and excess thionyl chloride were distilled off under reduced pressure. The residue was dissolved in tetrahydrofuran (10 ml). The solution was added dropwise at room temperature to tetrahydrofuran (15 ml) in which 2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylaniline (1.7 g) and pyridine (0.91 g) are dissolved, and the mixture was stirred overnight. The reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and 2 N hydrochloric acid, and then dried over anhydrous sodium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then purified by column chromatography to give 3-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4fluorobenzamide (1.7 g, yield 65%).

¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.31 (3H, s), 2.66 (2H, q), 7.35-7.40 (3H, m), 7.53 (1H, s), 8.17-8.25 (2H, m).

Step 12-2: Synthesis of 3-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 1-49).

According to the method of Synthetic example 2, the title compound was obtained from 3-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4fluorobenzamide which had been obtained in Step 12-1.

¹H-NMR: see the Table below.

Step 12-3: Synthesis of tert-butyl[5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]carbamoyl}-2-(1H-1,2,4-triazol-1-yl)benzyl]carbamate (Compound No. 12-1).

According to the method of Step 7-4 of Synthetic example 7, the title compound was obtained from 3-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluo-ropropan-2-yl)-6methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide which had been obtained in Step 12-2.

¹H-NMR: see the Table below.

Step 12-4: Synthesis of 3-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 12-2).

According to the method of Step 7-5 of Synthetic example 7, the title compound was obtained from tert-butyl [5-{[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]carbamoyl}-2-(1H-1,2,4-triazol-1-yl)benzyl]carbamate which had been obtained in Step 12-3.

¹H-NMR: see the Table below.

Step 12-5: Synthesis of 3-(acetamidemethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide (Compound No. 12-3).

According to the method of Step 6-4 of Synthetic example 6, the title compound was obtained from 3-(aminomethyl)-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6methylphenyl]-4-(1H-1,2,4-triazol-1-yl)benzamide which had been obtained in Step 12-4.

¹H-NMR: see the Table below.

Synthetic Example 13 Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methyl-phenyl]-4-[(propionylamino)methyl]-3-(1H-pyrazol-1-yl)benzamide (Compound No. 13-1).

Step 13-1: Synthesis of Methyl 4-cyano-3-(1H-pyrazol-1-yl)benzoate

Methyl 4-cyano-3-fluorobenzoate (0.30 g) and 1H-pyrazole (0.14 g) were dissolved in N,N-dimethylformamide (10 ml). To the reaction solution, sodium hydride (0.10 g) was added under ice cooling while stirring the mixture, and the mixture was stirred for 30 min. After increasing the temperature to room temperature, the solution was further stirred for 2 hours. The reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water, and then dried over anhydrous sodium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then purified by column chromatography to give methyl 4-cyano-3-(1H-pyrazol-1-yl)benzoate (0.28 g, yield 73%).

¹H-NMR (CDCl₃) δ: 3.99 (3H, s), 6.58 (1H, dd), 7.85-7.88 (2H, m), 8.06 (1H, dd), 8.18 (1H, dd), 8.43 (1H, d).

Step 13-2: Synthesis of 4-cyano-3-(1H-pyrazol-1-yl)benzoic Acid

Methyl 4-cyano-3-(1H-pyrazol-1-yl)benzoate (0.27 g) was dissolved in tetrahydrofuran (10 ml). To the solution, a solution in which lithium hydroxide monohydrate (0.10 g) is dissolved in water (10 ml) was added at room temperature. The reaction mixture was stirred for 2 hours. The reaction solution was acidified with 2 N hydrochloric acid, and then extracted twice with ethyl acetate. The organic phases were combined, washed with water, and then dried over anhydrous sodium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product of 4-cyano-3-(1H-pyrazol-1-yl)benzoic acid (0.23 g). The crude product was used for the next step without further purification.

¹H-NMR (DMSO-d₆) δ: 6.66 (1H, dd), 7.91 (1H, s), 8.02 (1H, d), 8.14 (1H, d), 8.22 (1H, s), 8.54 (1H, d).

Step 13-3: Synthesis of 4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-(1H-pyrazol-1-yl)benzamide (Compound No. 14-1).

The crude product of 4-cyano-3-(1H-pyrazol-1-yl)benzoic acid (0.23 g) was suspended in toluene (10 ml), thionyl chloride (0.64 g) and a small amount of N,N-dimethylformamide (2 to 3 drops) were added thereto, and the mixture was heated and stirred for 6 hours at reflux temperature. After cooling to room temperature, the solvent and excess thionyl chloride were distilled off under reduced pressure. To the residue, 4-dimethylaminopyridine (7 mg), pyridine (0.18 g) and 2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro propan-2-yl)-6-methylaniline (0.34 g) dissolved in tetrahydrofuran (15 ml) were added, and the mixture was stirred at room temperature for 3 hours. The mixture was further heated and stirred for 3 hours at reflux temperature. After cooling to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and a saturated sodium bicarbonate aqueous solution sequentially, and then dried over anhydrous sodium sulfate. The drying agent was removed by filtration, and the solvent was distilled off under reduced pressure to obtain a crude product, which was then purified by column chromatography to give 4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]-3-(1H-pyrazol-1-yl)benzamide (0.13 g, yield 23%).

¹H-NMR: see the Table below.

Step 13-4: Synthesis of N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-[(propionylamino)methyl]-3-(1H-pyrazol-1-yl)benzamide (Compound No. 13-1).

The title compound was obtained from 4-cyano-N-[2-ethyl-4-(1,1,1,2,3,3,3-heptafluoro-propan-2-yl)-6-methylphenyl]-3-(1H-pyrazol-1-yl)benzamide which had been obtained in Step 13-3 according to the method of Step 7-4 of Synthetic example 7 by using propionic anhydride instead of di-tert-butyl bicarbonate.

¹H-NMR (CDCl₃): see the Table below.

The compounds of Formula (I) of the present invention and intermediates thereof, that are obtained by the same methods as those of the above Synthetic examples or obtained in accordance with the methods described in detail above as well as their physical properties are set forth in Tables 1 to 14, Tables A to M and NMR Table below. The compounds obtained in the above Synthetic examples are also described in the corresponding tables.

TABLE 1

Exa R1 R2 J R4 R5 Q R7 R8 W 1-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H H 1H-pyrazol-1-yl 1-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H H 4-chloro-1H-pyrazol-1-yl 1-3 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H H 1H-1,2,4-triazol-1-yl 1-4 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ CH₃ H H 1H-1,2,4-triazol-1-yl 1-5 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H chloro H 1H-1,2,4-triazol-1-yl 1-6 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H trifluoro- H 1H-124-triazol-1-yl methyl 1-7 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H nitro H 1H-1,2,4-triazol-1-yl 1-8 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H chloro 1H-1,2,4-triazol-1-yl 1-9 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H bromo 1H-1,2,4-triazol-1-yl 1-10 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H trifluoromethyl 1H-1,2,4-triazol-1-yl 1-11 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H nitro 1H-1,2,4-triazol-1-yl 1-12 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H cyano 1H-1,2,4-triazol-1-yl 1-13 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H H 5-(ethylsulfanyl)-1H- tetrazol-1-yl 1-14 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-pyrrol-1-yl 1-15 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H trifluoromethyl 2-cyano-1H-pyrrol-1-yl 1-16 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-pyrazol-1-yl 1-17 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-pyrazol-1-yl 1-18 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H (phenylcarbonyl)- 1H-pyrazol-1-yl amino 1-19 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(2-fluorophenyl))- 1H-pyrazol-1-yl carbonyl]amino 1-20 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(2-chloropyridin-3- 1H-pyrazol-1-yl yl)carbonyl]amino 1-21 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 4-chloro-1H-pyrazol-1-yl 1-22 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 4-(trifluoromethyl)-1H- pyrazol-1-yl 1-23 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 4-nitro-1H-pyrazol-1-yl 1-24 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 4-cyano-1H-pyrazol-1-yl 1-25 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-imidazol-1-yl 1-26 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-imidazol-1-yl 1-27 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-1,2,3-triazol-1-yl 1-28 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-1,2,3-triazol-1-yl 1-29 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 2H-1,2,3-triazol-2-yl 1-30 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 2H-1,2,3-triazol-2-yl 1-31 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-1,2,4-triazol-1-yl 1-32 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ 1H-1,2,4-triazol-1-yl 1-33 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H trifluoromethyl 1H-1,2,4-triazol-1-yl 1-34 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H fluoro 1H-1,2,4-triazol-1-yl 1-35 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H chloro 1H-1,2,4-triazol-1-yl 1-36 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H bromo 1H-1,2,4-triazol-1-yl 1-37 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H methoxy 1H-1,2,4-triazol-1-yl 1-38 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H amino 1H-1,2,4-triazol-1-yl 1-39 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-1,2,4-triazol-1-yl 1-40 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H propanoylamino 1H-1,2,4-triazol-1-yl 1-41 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H (phenylcarbonyl)- 1H-1,2,4-triazol-1-yl amino 1-42 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(2-fluorophenyl)- 1H-1,2,4-triazol-1-yl carbonyl]amino 1-43 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(4-fluorophenyl)- 1H-1,2,4-triazol-1-yl carbonyl]amino 1-44 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(2,5-difluorophenyl)- 1H-1,2,4-triazol-1-yl carbonyl]amino 1-45 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(2-fluoropyridin-3- 1H-1,2,4-triazol-1-yl yl)carbonyl]amino 1-46 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H [(2-chloropyridin-3- 1H-1,2,4-triazol-1-yl yl)carbonyl]amino 1-47 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H (methoxycarbonyl)- 1H-1,2,4-triazol-1-yl amino 1-48 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H (methylsulfonyl)- 1H-1,2,4-triazol-1-yl amino 1-49 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H cyano 1H-1,2,4-triazol-1-yl 1-50 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 3-(trifluoromethyl)- 1H-1,2,4-triazol-1-yl 1-51 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H amino 3-(trifluoromethyl)- 1H-1,2,4-triazol-1-yl 1-52 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 3-(trifluoromethyl)- 1H-1,2,4-triazol-1-yl 1-53 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 3-(methoxycarbonyl)- 1H-1,2,4-triazol-1-yl 1-54 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 3-carbamoyl-1H- 1,2,4-triazol-1-yl 1-55 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-tetrazol-1-yl 1-56 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H fluoro H 1H-tetrazol-1-yl 1-57 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-tetrazol-1-yl 1-58 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 2H-tetrazol-2-yl 1-59 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 2H-tetrazol-2-yl 1-60 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 5-(methylsulfanyl)- 1H-tetrazol-1-yl 1-61 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-benzotriazol-1-yl 1-62 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-benzotriazol-1-yl 1-63 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 2H-benzotriazol-2-yl 1-64 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H propan-2- H H H 1H-1,2,4-triazol-1-yl yl 1-65 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H propan-2- H H amino 1H-1,2,4-triazol-1-yl yl 1-66 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H propan-2- H H nitro 1H-1,2,4-triazol-1-yl yl 1-67 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H methoxy- H H H 1H-1,2,4-triazol-1-yl methyl 1-68 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H methoxy- H H amino 1H-1,2,4-triazol-1-yl methyl 1-69 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H methoxy- H H nitro 1H-1,2,4-triazol-1-yl methyl 1-70 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H methoxy H H H 1H-1,2,4-triazol-1-yl 1-71 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H methoxy H H amino 1H-1,2,4-triazol-1-yl 1-72 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H methoxy H H nitro 1H-1,2,4-triazol-1-yl 1-73 ethyl H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 1H-1,2,4-triazol-1-yl 1-74 ethyl H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H chloro 1H-1,2,4-triazol-1-yl 1-75 ethyl H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H bromo 1H-1,2,4-triazol-1-yl 1-76 ethyl H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H amino 1H-1,2,4-triazol-1-yl 1-77 ethyl H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H nitro 1H-1,2,4-triazol-1-yl 1-78 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H 1H-1,2,4-triazol-1-yl 1-79 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H (trifluoro- H H H 1H-1,2,4-triazol-1-yl methyl)- sulfanyl 1-80 iodo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H iodo H H H 1H-1,2,4-triazol-1-yl 1-81 iodo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H iodo H H nitro 1H-1,2,4-triazol-1-yl 1-82 CH₃ H 2-chloro-1,1,1,3,3,3- H ethyl H H H 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl 1-83 CH₃ H 1,1,1,3,3,3-hexafluoro- H ethyl H H H 1H-1,2,4-triazol-1-yl 2-hydroxypropan-2-yl 1-84 CH₃ H (2-ethoxy-1,1,1,3,3,3- H ethyl H H H 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl 1-85 CH₃ H 1,1,1,3,3,3-hexafluoro-2- H ethyl H H H 1H-1,2,4-triazol-1-yl [(methylsulfonyl)oxy]- propan-2-yl 1-86 CH₃ H 2-(4-chloro-1H-pyrazol-1-yl)- H ethyl H H H 1H-tetrazol-1-yl 1,1,1,3,3,3-hexafluoropropan-2-yl 1-87 CH₃ H 1,1,1,3,3,3-hexafluoro-2- H CH₃ H chloro H 1H-1,2,4-triazol-1-yl (1H-1,2,4-triazol-1-yl)- propan-2-yl 1-88 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H H 1H-1,2,4-triazol-1-yl 1-89 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H 1H-1,2,4-triazol-1-yl 1-90 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H 1H-1,2,4-triazol-1-yl 1-91 iodo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H iodo H H H 1H-1,2,4-triazol-1-yl 1-92 CH₃ H undecafluorocyclohexyl H CH₃ H H H 1H-1,2,4-triazol-1-yl 1-93 CH₃ H undecafluorocyclohexyl H ethyl H H H 1H-1,2,4-triazol-1-yl 1-94 bromo H undecafluorocyclohexyl H bromo H H H 1H-1,2,4-triazol-1-yl 1-95 iodo H undecafluorocyclohexyl H iodo H H H 1H-1,2,4-triazol-1-yl 1-96 CH₃ H undecafluorocyclohexyl H ethyl H H bromo 1H-1,2,4-triazol-1-yl 1-97 bromo H trifluoromethoxy H bromo H H H 1H-1,2,4-triazol-1-yl 1-98 bromo H trifluoromethylsulfanyl H bromo H H H 1H-1,2,4-triazol-1-yl 1-99 CH₃ H (pentafluoroethyl)sulfanyl H ethyl H H H 1H-1,2,4-triazol-1-yl 1-100 CH₃ H (pentafluoroethyl)sulfanyl H ethyl H H amino 1H-1,2,4-triazol-1-yl 1-101 CH₃ H (pentafluoroethyl)sulfanyl H ethyl H H nitro 1H-1,2,4-triazol-1-yl 1-102 CH₃ H (pentafluoroethyl)sulfanyl H ethyl H H propanoylamino 1H-1,2,4-triazol-1-yl 1-103 CH₃ H (pentafluoroethyl)sulfanyl H ethyl H H [(2-fluorophenyl))- 1H-1,2,4-triazol-1-yl carbonyl]amino 1-104 CH₃ H (pentafluoroethyl)sulfanyl H ethyl H H (methoxycarbonyl)- 1H-1,2,4-triazol-1-yl amino 1-105 bromo H (pentafluoroethyl)sulfanyl H bromo H H H 1H-1,2,4-triazol-1-yl 1-106 bromo H (heptafluoropropyl)- H bromo H H H 1H-1,2,4-triazol-1-yl sulfanyl 1-107 bromo H (nonafluorobutyl)sulfanyl H bromo H H H 1H-1,2,4-triazol-1-yl 1-108 unused number 1-109 unused number 1-110 unused number 1-111 unused number 1-112 unused number 1-113 unused number 1-114 unused number 1-115 unused number 1-116 unused number 1-117 unused number 1-118 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H cyano 1H-1,2,4-triazol-1-yl 1-119 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H cyano 1H-1,2,4-triazol-1-yl 1-120 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H H 1H-1,2,4-triazol-1-yl 2-yl 1-121 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H H 1H-1,2,4-triazol-1-yl 2-yl 1-122 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H bromo H H H 1H-1,2,4-triazol-1-yl 2-yl 1-123 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoro- H H H 1H-1,2,4-triazol-1-yl 2-yl methoxy 1-124 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H cyano 1H-1,2,4-triazol-1-yl 2-yl 1-125 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H cyano 1H-1,2,4-triazol-1-yl 2-yl 1-126 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoro- H H H 1H-1,2,4-triazol-1-yl methoxy 1-127 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoro- H H H 1H-1,2,4-triazol-1-yl methoxy 1-128 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoro- H H H 1H-1,2,4-triazol-1-yl methoxy 1-129 CH H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoro- H H H 1H-1,2,4-triazol-1-yl methoxy 1-130 CH H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoro- H H H 1H-1,2,4-triazol-1yl methoxy 1-131 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoro- H H H 1H-1,2,4-triazol-1-yl 2-yl methoxy 1-132 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoro- H H H 1H-1,2,4-triazol-1-yl methoxy 1-133 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan- H difluoro- H H H 1H-1,2,4-triazol- -yl 2-yl methoxy 1-134 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoro- H H H 1H-1,2,4-triazol-1-yl 2-yl methoxy

TABLE 2

Exa R1 R2 J R4 R5 Q W 2-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H 1H-1,2,4-triazol-1-yl 2-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H 1H-1,2,4-triazol-1-yl 2-3 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H 1H-1,2,4-triazol-1-yl 2-4 CH₃ H 1,1,1,3,3,3-hexafluoro-2-(1H-1,2,4-triazol-1-yl)propan-2-yl H ethyl H 1H-1,2,4-triazol-1-yl 2-5 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H 1H-1,2,4-triazol-1-yl 2-6 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H 1H-1,2,4-triazol-1-yl 2-7 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H 1H-1,2,4-triazol-1-yl 2-8 iodo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H iodo H 1H-1,2,4-triazol-1-yl 2-9 CH₃ H undecafluorocyclohexyl H CH₃ H 1H-1,2,4-triazol-1-yl 2-10 CH₃ H undecafluorocyclohexyl H ethyl H 1H-1,2,4-triazol-1-yl 2-11 bromo H undecafluorocyclohexyl H bromo H 1H-1,2,4-triazol-1-yl 2-12 iodo H undecafluorocyclohexyl H iodo H 1H-1,2,4-triazol-1-yl 2-13 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H 1H-1,2,4-triazol-1-yl 2-14 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H 1H-1,2,4-triazol-1-yl 2-15 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H 1H-1,2,4-triazol-1-yl 2-16 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-17 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-18 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-19 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-20 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-21 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-22 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-23 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl 2-24 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H 1H-1,2,4-triazol-1-yl

TABLE 3

Exa R1 R2 J R4 R5 Q R8 W 3-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H 1H-1,2,4-triazol-1-yl 3-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl 3-3 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H 1H-1,2,4-triazol-1-yl 3-4 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H 1H-1,2,4-triazol-1-yl 3-5 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl 3-6 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H 1H-1,2,4-triazol-1-yl 3-7 iodo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H iodo H H 1H-1,2,4-triazol-1-yl 3-8 CH₃ H undecafluorocyclohexyl H CH₃ H H 1H-1,2,4-triazol-1-yl 3-9 CH₃ H undecafluorocyclohexyl H ethyl H H 1H-1,2,4-triazol-1-yl 3-10 bromo H undecafluorocyclohexyl H bromo H H 1H-1,2,4-triazol-1-yl 3-11 iodo H undecafluorocyclohexyl H iodo H H 1H-1,2,4-triazol-1-yl 3-12 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H 1H-1,2,4-triazol-1-yl 3-13 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl 3-14 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H 1H-1,2,4-triazol-1-yl 3-15 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-16 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-17 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-18 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-19 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-20 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-21 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-22 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 3-23 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl

TABLE 4

Exa R1 R2 J R4 R5 Q R7 W 4-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H 1H-1,2,4-triazol-1-yl 4-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl 4-3 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H 1H-1,2,4-triazol-1-yl 4-4 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H 1H-1,2,4-triazol-1-yl 4-5 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl 4-6 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H 1H-1,2,4-triazol-1-yl 4-7 iodo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H iodo H H 1H-1,2,4-triazol-1-yl 4-8 CH₃ H undecafluorocyclohexyl H CH₃ H H 1H-1,2,4-triazol-1-yl 4-9 CH₃ H undecafluorocyclohexyl H ethyl H H 1H-1,2,4-triazol-1-yl 4-10 bromo H undecafluorocyclohexyl H bromo H H 1H-1,2,4-triazol-1-yl 4-11 iodo H undecafluorocyclohexyl H iodo H H 1H-1,2,4-triazol-1-yl 4-12 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H 1H-1,2,4-triazol-1-yl 4-13 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl 4-14 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H 1H-1,2,4-triazol-1-yl 4-15 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-16 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-17 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-18 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-19 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-20 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-21 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-22 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl 4-23 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 1H-1,2,4-triazol-1-yl

TABLE 5

Exa R1 R2 J R4 R5 Q R7 R8 R10 R14 R15 5-1 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H H heptafluoropropan-2-yl 5-2 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H acetyl heptafluoropropan-2-yl 5-3 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H propanoyl heptafluoropropan-2-yl 5-4 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H 2-methylpropanoyl heptafluoropropan-2-yl 5-5 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H chloroacetyl heptafluoropropan-2-yl 5-6 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H difluoroacetyl heptafluoropropan-2-yl 5-7 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-8 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H cyclopropylacetyl heptafluoropropan-2-yl 5-9 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H cyclobutylcarbonyl heptafluoropropan-2-yl 5-10 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H cyclopentylcarbonyl heptafluoropropan-2-yl 5-11 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H cyclohexylcarbonyl heptafluoropropan-2-yl 5-12 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H (2E)-but-2-enoyl heptafluoropropan-2-yl 5-13 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H (2E)-2-methylbut- heptafluoropropan-2-yl 2-enoyl 5-14 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H methoxyacetyl heptafluoropropan-2-yl 5-15 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H 3-methoxy- heptafluoropropan-2-yl propanoyl 5-16 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H 3-methoxybutanoyl heptafluoropropan-2-yl 5-17 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H 1H-1,2,4-triazol- heptafluoropropan-2-yl 1-ylacetyl 5-18 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H (4-fluorophenyl)- heptafluoropropan-2-yl acetyl 5-19 CH₃ H 1,1,1,2,3,3,3- H CH₃ H H H H H (2-fluoropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-20 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H H heptafluoropropan-2-yl 5-21 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H acetyl heptafluoropropan-2-yl 5-22 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H propanoyl heptafluoropropan-2-yl 5-23 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-24 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H cyclopropylacetyl heptafluoropropan-2-yl 5-25 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-26 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-27 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H H heptafluoropropan-2-yl 5-28 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H acetyl heptafluoropropan-2-yl 5-29 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H propanoyl heptafluoropropan-2-yl 5-30 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-31 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H cyclopropylacetyl heptafluoropropan-2-yl 5-32 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-33 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (methylsulfanyl)- heptafluoropropan-2-yl acetyl 5-34 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (2-fluorophenyl)- heptafluoropropan-2-yl carbonyl 5-35 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (3-fluorophenyl)- heptafluoropropan-2-yl carbonyl 5-36 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (4-fluorophenyl)- heptafluoropropan-2-yl carbonyl 5-37 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (2-chlorophenyl)- heptafluoropropan-2-yl carbonyl 5-38 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (3-chlorophenyl)- heptafluoropropan-2-yl carbonyl 5-39 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (4-chlorophenyl)- heptafluoropropan-2-yl carbonyl 5-40 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (2-fluoropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-41 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (2-chloropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-42 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H (2,2,2-trichloro- heptafluoropropan-2-yl ethoxy)carbonyl 5-43 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H H heptafluoropropan-2-yl 5-44 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H acetyl heptafluoropropan-2-yl 5-45 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H propanoyl heptafluoropropan-2-yl 5-46 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H cyclopropylacetyl heptafluoropropan-2-yl 5-47 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-48 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H (2-fluoropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-49 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H H H tert-butoxycarbonyl heptafluoropropan-2-yl 5-50 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H H heptafluoropropan-2-yl 5-51 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H acetyl heptafluoropropan-2-yl 5-52 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H propanoyl heptafluoropropan-2-yl 5-53 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-54 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H cyclopropylacetyl heptafluoropropan-2-yl 5-55 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-56 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro fluoro H H tert-butoxycarbonyl heptafluoropropan-2-yl 5-57 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H H heptafluoropropan-2-yl 5-58 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H acetyl heptafluoropropan-2-yl 5-59 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H propanoyl heptafluoropropan-2-yl 5-60 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H cyclopropylcarbonyl heptafluoropropan-2-yl 5-61 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H cyclopropylacetyl heptafluoropropan-2-yl 5-62 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-63 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H tert-butoxycarbonyl heptafluoropropan-2-yl 5-64 CH₃ H 1,1,1,2,3,3,3- H ethyl H chloro H H H H heptafluoropropan-2-yl 5-65 CH₃ H 1,1,1,2,3,3,3- H ethyl H chloro H H H acetyl heptafluoropropan-2-yl 5-66 CH₃ H 1,1,1,2,3,3,3- H ethyl H chloro H H H propanoyl heptafluoropropan-2-yl 5-67 CH₃ H 1,1,1,2,3,3,3- H ethyl H chloro H H H cyclopropylacetyl heptafluoropropan-2-yl 5-68 CH₃ H 1,1,1,2,3,3,3- H ethyl H chloro H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-69 CH₃ H 1,1,1,2,3,3,3- H ethyl H chloro H H H tert-butoxycarbonyl heptafluoropropan-2-yl 5-70 CH₃ H 1,1,1,2,3,3,3- H ethyl H H fluoro H H H heptafluoropropan-2-yl 5-71 CH₃ H 1,1,1,2,3,3,3- H ethyl H H fluoro H H acetyl heptafluoropropan-2-yl 5-72 CH₃ H 1,1,1,2,3,3,3- H ethyl H H fluoro H H propanoyl heptafluoropropan-2-yl 5-73 CH₃ H 1,1,1,2,3,3,3- H ethyl H H fluoro H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-74 CH₃ H 1,1,1,2,3,3,3- H ethyl H H fluoro H H cyclopropylacetyl heptafluoropropan-2-yl 5-75 CH₃ H 1,1,1,2,3,3,3- H ethyl H H fluoro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-76 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H H heptafluoropropan-2-yl 5-77 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H acetyl heptafluoropropan-2-yl 5-78 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H propanoyl heptafluoropropan-2-yl 5-79 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-80 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H cyclopropylacetyl heptafluoropropan-2-yl 5-81 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-82 CH₃ H 1,1,1,2,3,3,3- H ethyl H H chloro H H (2-fluoropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-83 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H H heptafluoropropan-2-yl 5-84 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H formyl heptafluoropropan-2-yl 5-85 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H acetyl heptafluoropropan-2-yl 5-86 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H propanoyl heptafluoropropan-2-yl 5-87 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-88 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H cyclopropylacetyl heptafluoropropan-2-yl 5-89 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-90 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (2E)-but-2-enoyl heptafluoropropan-2-yl 5-91 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H methoxyacetyl heptafluoropropan-2-yl 5-92 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (4-fluorophenyl)- heptafluoropropan-2-yl carbonyl 5-93 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (2-fluoropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-94 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (2-chloropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-95 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H ethylcarbamoyl heptafluoropropan-2-yl 5-96 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H methylsulfonyl heptafluoropropan-2-yl 5-97 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H dimethylsulfamoyl heptafluoropropan-2-yl 5-98 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H H heptafluoropropan-2-yl 5-99 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H acetyl heptafluoropropan-2-yl 5-100 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H propanoyl heptafluoropropan-2-yl 5-101 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H cyclopropylacetyl heptafluoropropan-2-yl 5-102 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-103 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H (2-fluoropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-104 CH₃ H 1,1,1,2,3,3,3- H ethyl H H CH₃ H H tert-butoxycarbonyl heptafluoropropan-2-yl 5-105 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H H heptafluoropropan-2-yl methyl 5-106 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H acetyl heptafluoropropan-2-yl methyl 5-107 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H propanoyl heptafluoropropan-2-yl methyl 5-108 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H cyclopropylcarbonyl heptafluoropropan-2-yl methyl 5-109 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H cyclopropylacetyl heptafluoropropan-2-yl methyl 5-110 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H 3,3,3-trifluoro- heptafluoropropan-2-yl methyl propanoyl 5-111 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H (4-fluorophenyl)- heptafluoropropan-2-yl methyl carbonyl 5-112 CH₃ H 1,1,1,2,3,3,3- H ethyl H H trifluoro- H H (2-fluoropyridin- heptafluoropropan-2-yl methyl 3-yl)carbonyl 5-113 CH₃ H 1,1,1,2,3,3,3- H ethyl H H nitoro H H H heptafluoropropan-2-yl 5-114 CH₃ H 1,1,1,2,3,3,3- H ethyl H H nitoro H H acetyl heptafluoropropan-2-yl 5-115 CH₃ H 1,1,1,2,3,3,3- H ethyl H H nitoro H H propanoyl heptafluoropropan-2-yl 5-116 CH₃ H 1,1,1,2,3,3,3- H ethyl H H nitoro H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-117 CH₃ H 1,1,1,2,3,3,3- H ethyl H H nitoro H H cyclopropylacetyl heptafluoropropan-2-yl 5-118 CH₃ H 1,1,1,2,3,3,3- H ethyl H H nitoro H H 3,3,3- heptafluoropropan-2-yl trifluoropropanoyl 5-119 bromo H 1,1,1,2,3,3,3- H bromo H H H H H H heptafluoropropan-2-yl 5-120 bromo H 1,1,1,2,3,3,3- H bromo H H H H H acetyl heptafluoropropan-2-yl 5-121 bromo H 1,1,1,2,3,3,3- H bromo H H H H H propanoyl heptafluoropropan-2-yl 5-122 bromo H 1,1,1,2,3,3,3- H bromo H H H H H cyclopropylcarbonyl heptafluoropropan-2-yl 5-123 bromo H 1,1,1,2,3,3,3- H bromo H H H H H cyclopropylacetyl heptafluoropropan-2-yl 5-124 bromo H 1,1,1,2,3,3,3- H bromo H H H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-125 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H H H H H nonafluorobutan-2-yl 5-126 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H H H H acetyl nonafluorobutan-2-yl 5-127 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H H H H propanoyl nonafluorobutan-2-yl 5-128 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H H H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-129 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H H H H cyclopropylacetyl nonafluorobutan-2-yl 5-130 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H H H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-131 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H chloro H H H nonafluorobutan-2-yl 5-132 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H chloro H H acetyl nonafluorobutan-2-yl 5-133 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H chloro H H propanoyl nonafluorobutan-2-yl 5-134 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H chloro H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-135 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H chloro H H cyclopropylacetyl nonafluorobutan-2-yl 5-136 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-137 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H H nonafluorobutan-2-yl 5-138 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H acetyl nonafluorobutan-2-yl 5-139 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H propanoyl nonafluorobutan-2-yl 5-140 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-141 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H cyclopropylacetyl nonafluorobutan-2-yl 5-142 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-143 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H H nonafluorobutan-2-yl 5-144 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H acetyl nonafluorobutan-2-yl 5-145 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H propanoyl nonafluorobutan-2-yl 5-146 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-147 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H cyclopropylacetyl nonafluorobutan-2-yl 5-148 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-149 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H H nonafluorobutan-2-yl 5-150 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H acetyl nonafluorobutan-2-yl 5-151 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H propanoyl nonafluorobutan-2-yl 5-152 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-153 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H cyclopropylacetyl nonafluorobutan-2-yl 5-154 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-155 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H chloro H H (2-fluoropyridin- nonafluorobutan-2-yl 3-yl)carbonyl 5-156 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H H nonafluorobutan-2-yl 5-157 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H acetyl nonafluorobutan-2-yl 5-158 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H propanoyl nonafluorobutan-2-yl 5-159 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-160 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H cyclopropylacetyl nonafluorobutan-2-yl 5-161 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-162 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H H H H H nonafluorobutan-2-yl 5-163 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H H H H acetyl nonafluorobutan-2-yl 5-164 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H H H H propanoyl nonafluorobutan-2-yl 5-165 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H H H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-166 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H H H H cyclopropylacetyl nonafluorobutan-2-yl 5-167 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H H H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-168 CH₃ H undecafluorocyclohexyl H ethyl H H chloro H H H 5-169 CH₃ H undecafluorocyclohexyl H ethyl H H chloro H H acetyl 5-170 CH₃ H undecafluorocyclohexyl H ethyl H H chloro H H propanoyl 5-171 CH₃ H undecafluorocyclohexyl H ethyl H H chloro H H cyclopropylcarbonyl 5-172 CH₃ H undecafluorocyclohexyl H ethyl H H chloro H H cyclopropylacetyl 5-173 CH₃ H undecafluorocyclohexyl H ethyl H H chloro H H 3,3,3-trifluoro- propanoyl 5-174 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H fluoro H H (2-fluoropyridin- nonafluorobutan-2-yl 3-yl)carbonyl 5-175 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H bromo H H (2-chloropyridin- nonafluorobutan-2-yl 3-yl)carbonyl 5-176 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (methylsulfanyl)- heptafluoropropan-2-yl acetyl 5-177 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (methylsulfinyl)- heptafluoropropan-2-yl acetyl 5-178 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (methylsulfonyl)- heptafluoropropan-2-yl acetyl 5-179 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (methylsulfanyl)- nonafluorobutan-2-yl acetyl 5-180 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (methylsulfinyl)- nonafluorobutan-2-yl acetyl 5-181 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (methylsulfonyl)- nonafluorobutan-2-yl acetyl 5-182 CH₃ H 1,1,1,2,3,3,3- H CH₃ H fluoro H H H (2-chloropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-183 CH₃ H 1,1,1,2,3,3,3- H ethyl H fluoro H fluoro H (2-chloropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-184 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H CH₃ H heptafluoropropan-2-yl 5-185 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H CH₃ acetyl heptafluoropropan-2-yl 5-186 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H CH₃ propanoyl heptafluoropropan-2-yl 5-187 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H CH₃ cyclopropylacetyl heptafluoropropan-2-yl 5-188 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H CH₃ 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-189 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H CH₃ (2-chloropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-190 CH3 H 1,1,1,2,3,3,3- H ethyl H H iodo H H acetyl heptafluoropropan-2-yl 5-191 CH3 H 1,1,1,2,3,3,3- H ethyl H H iodo H H propanoyl heptafluoropropan-2-yl 5-192 CH3 H 1,1,1,2,3,3,3- H ethyl H H iodo H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-193 CH3 H 1,1,1,2,3,3,4,4,4- H ethyl H H iodo H H H nonafluorobutan-2-yl 5-194 CH3 H 1,1,1,2,3,3,4,4,4- H ethyl H H iodo H H acetyl nonafluorobutan-2-yl 5-195 CH3 H 1,1,1,2,3,3,4,4,4- H ethyl H H iodo H H propanoyl nonafluorobutan-2-yl 5-196 CH3 H 1,1,1,2,3,3,4,4,4- H ethyl H H iodo H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-197 CH3 H 1,1,1,2,3,3,4,4,4- H ethyl H H iodo H H cyclopropylacetyl nonafluorobutan-2-yl 5-198 CH3 H 1,1,1,2,3,3,4,4,4- H ethyl H H iodo H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-199 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H (2-chloropyridin- heptafluoropropan-2-yl 3-yl)carbonyl 5-200 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H H nonafluorobutan-2-yl 5-201 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H acetyl nonafluorobutan-2-yl 5-202 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H propanoyl nonafluorobutan-2-yl 5-203 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H cyclopropylcarbonyl nonafluorobutan-2-yl 5-204 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H cyclopropylacetyl nonafluorobutan-2-yl 5-205 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-206 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H fluoro fluoro H H (2-chloropyridin- nonafluorobutan-2-yl 3-yl)carbonyl 5-207 unused number 5-208 unused number 5-209 unused number 5-210 CH3 H 1,1,1,2,3,3,4,4,4- H CH3 H H bromo H H H nonofluorobutan-2-yl 5-211 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H bromo H H acetyl nonofluorobutan-2-yl 5-212 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H H bromo H H propanoyl nonofluorobutan-2-yl 5-213 CH₃ H 1,1,1,2,3,3,4,4,4- H CH₃ H fluoro fluoro H H 3,3,3-trifluoro- nonofluorobutan-2-yl propanoyl 5-214 CH₃ H 1-bromo-1,1,2,3,3,3- H CH₃ H H chloro H H H hexafluoropropan-2-yl 5-215 CH₃ H 1-bromo-1,1,2,3,3,3- H CH₃ H H chloro H H acetyl hexafluoropropan-2-yl 5-216 CH₃ H 1-bromo-1,1,2,3,3,3- H CH₃ H H chloro H H propanoyl hexafluoropropan-2-yl 5-217 CH₃ H 1-bromo-1,1,2,3,3,3- H CH₃ H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-218 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H chloro H H H hexafluoropropan-2-yl 5-219 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H chloro H H acetyl hexafluoropropan-2-yl 5-220 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H chloro H H propanoyl hexafluoropropan-2-yl 5-221 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-222 chloro H 1,1,1,2,3,3,3- H chloro H H H H H H heptafluoropropan-2-yl 5-223 chloro H 1,1,1,2,3,3,3- H chloro H H H H H acetyl heptafluoropropan-2-yl 5-224 chloro H 1,1,1,2,3,3,3- H chloro H H H H H propanoyl heptafluoropropan-2-yl 5-225 chloro H 1,1,1,2,3,3,3- H chloro H H H H H cyclopropyl-acetyl heptafluoropropan-2-yl 5-226 chloro H 1,1,1,2,3,3,3- H chloro H H H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-227 chloro H 1,1,1,2,3,3,3- H chloro H H H H H tert-butoxy- heptafluoropropan-2-yl carbonyl 5-228 chloro H 1,1,1,2,3,3,3- H chloro H H chloro H H H heptafluoropropan-2-yl 5-229 chloro H 1,1,1,2,3,3,3- H chloro H H chloro H H acetyl heptafluoropropan-2-yl 5-230 chloro H 1,1,1,2,3,3,3- H chloro H H chloro H H propanoyl heptafluoropropan-2-yl 5-231 chloro H 1,1,1,2,3,3,3- H chloro H H chloro H H cyclopropyl- heptafluoropropan-2-yl carbonyl 5-232 chloro H 1,1,1,2,3,3,3- H chloro H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-233 bromo H 1,1,1,2,3,3,3- H bromo H H chloro H H H heptafluoropropan-2-yl 5-234 bromo H 1,1,1,2,3,3,3- H bromo H H chloro H H acetyl heptafluoropropan-2-yl 5-235 bromo H 1,1,1,2,3,3,3- H bromo H H chloro H H propanoyl heptafluoropropan-2-yl 5-236 bromo H 1,1,1,2,3,3,3- H bromo H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-237 iodo H 1,1,1,2,3,3,3- H iodo H H chloro H H H heptafluoropropan-2-yl 5-238 iodo H 1,1,1,2,3,3,3- H iodo H H chloro H H acetyl heptafluoropropan-2-yl 5-239 iodo H 1,1,1,2,3,3,3- H iodo H H chloro H H propanoyl heptafluoropropan-2-yl 5-240 iodo H 1,1,1,2,3,3,3- H iodo H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-241 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H H nonafluorobutan-2-yl 5-242 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H acetyl nonafluorobutan-2-yl 5-243 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H propanoyl nonafluorobutan-2-yl 5-244 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-245 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H chloro H H H nonafluorobutan-2-yl 5-246 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H chloro H H acetyl nonafluorobutan-2-yl 5-247 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H chloro H H propanoyl nonafluorobutan-2-yl 5-248 bromo H 1,1,1,2,3,3,4,4,4- H bromo H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-249 bromo H 1,1,1,2,3,3,4,4,4- H difluoro- H H chloro H H H nonafluorobutan-2-yl methoxy 5-250 bromo H 1,1,1,2,3,3,4,4,4- H difluoro- H H chloro H H acetyl nonafluorobutan-2-yl methoxy 5-251 bromo H 1,1,1,2,3,3,4,4,4- H difluoro- H H chloro H H propanoyl nonafluorobutan-2-yl methoxy 5-252 bromo H 1,1,1,2,3,3,4,4,4- H difluoro- H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl methoxy propanoyl 5-253 bromo H 1,1,1,2,3,3,4,4,4- H trifluoro- H H chloro H H H nonafluorobutan-2-yl methoxy 5-254 bromo H 1,1,1,2,3,3,4,4,4- H trifluoro- H H chloro H H acetyl nonafluorobutan-2-yl methoxy 5-255 bromo H 1,1,1,2,3,3,4,4,4- H trifluoro- H H chloro H H propanoyl nonafluorobutan-2-yl methoxy 5-256 bromo H 1,1,1,2,3,3,4,4,4- H trifluoro- H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl methoxy propanoyl 5-257 bromo H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H H nonafluorobutan-2-yl sulfanyl 5-258 bromo H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H acetyl nonafluorobutan-2-yl sulfanyl 5-259 bromo H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H propanoyl nonafluorobutan-2-yl sulfanyl 5-260 bromo H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl sulfanyl propanoyl 5-261 bromo H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl)- H H chloro H H H nonafluorobutan-2-yl sulfanyl 5-262 bromo H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl)- H H chloro H H acetyl nonafluorobutan-2-yl sulfanyl 5-263 bromo H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl)- H H chloro H H propanoyl nonafluorobutan-2-yl sulfanyl 5-264 bromo H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl)- H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl sulfanyl propanoyl 5-265 iodo H 1,1,1,2,3,3,4,4,4- H iodo H H chloro H H H nonafluorobutan-2-yl 5-266 iodo H 1,1,1,2,3,3,4,4,4- H iodo H H chloro H H acetyl nonafluorobutan-2-yl 5-267 iodo H 1,1,1,2,3,3,4,4,4- H iodo H H chloro H H propanoyl nonafluorobutan-2-yl 5-268 iodo H 1,1,1,2,3,3,4,4,4- H iodo H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-269 chloro H 1-bromo-1,1,2,3,3,3- H chloro H H chloro H H H hexafluoropropan-2-yl 5-270 chloro H 1-bromo-1,1,2,3,3,3- H chloro H H chloro H H acetyl hexafluoropropan-2-yl 5-271 chloro H 1-bromo-1,1,2,3,3,3- H chloro H H chloro H H propanoyl hexafluoropropan-2-yl 5-272 chloro H 1-bromo-1,1,2,3,3,3- H chloro H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-273 bromo H 1-bromo-1,1,2,3,3,3- H bromo H H chloro H H H hexafluoropropan-2-yl 5-274 bromo H 1-bromo-1,1,2,3,3,3- H bromo H H chloro H H acetyl hexafluoropropan-2-yl 5-275 bromo H 1-bromo-1,1,2,3,3,3- H bromo H H chloro H H propanoyl hexafluoropropan-2-yl 5-276 bromo H 1-bromo-1,1,2,3,3,3- H bromo H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-277 iodo H 1-bromo-1,1,2,3,3,3- H iodo H H chloro H H H hexafluoropropan-2-yl 5-278 iodo H 1-bromo-1,1,2,3,3,3- H iodo H H chloro H H acetyl hexafluoropropan-2-yl 5-279 iodo H 1-bromo-1,1,2,3,3,3- H iodo H H chloro H H propanoyl hexafluoropropan-2-yl 5-280 iodo H 1-bromo-1,1,2,3,3,3- H iodo H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-281 bromo H pentafluoroethyl H difluoromethoxy H H chloro H H H 5-282 bromo H pentafluoroethyl H difluoromethoxy H H chloro H H acetyl 5-283 bromo H pentafluoroethyl H difluoromethoxy H H chloro H H propanoyl 5-284 bromo H pentafluoroethyl H difluoromethoxy H H chloro H H 3,3,3-trifluoro- propanoyl 5-285 bromo H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H H eptafluoropropan-2-yl 5-286 bromo H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H acetyl heptafluoropropan-2-yl 5-287 bromo H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H propanoyl heptafluoropropan-2-yl 5-288 bromo H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-289 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H H hexafluoropropan-2-yl 5-290 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H acetyl hexafluoropropan-2-yl 5-291 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H propanoyl hexafluoropropan-2-yl 5-292 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-293 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H H heptafluoropropan-2-yl 5-294 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H acetyl heptafluoropropan-2-yl 5-295 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H propanoyl heptafluoropropan-2-yl 5-296 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-297 CH₃ H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H H nonafluorobutan-2-yl 5-298 CH₃ H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H acetyl nonafluorobutan-2-yl 5-299 CH₃ H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H propanoyl nonafluorobutan-2-yl 5-300 CH₃ H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-301 CH₃ H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H H hexafluoropropan-2-yl 5-302 CH₃ H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H acetyl hexafluoropropan-2-yl 5-303 CH₃ H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H propanoyl hexafluoropropan-2-yl 5-304 CH₃ H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-305 chloro H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H H heptafluoropropan-2-yl 5-306 chloro H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H acetyl heptafluoropropan-2-yl 5-307 chloro H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H propanoyl heptafluoropropan-2-yl 5-308 chloro H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-309 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H H nonafluorobutan-2-yl 5-310 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H acetyl nonafluorobutan-2-yl 5-311 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H propanoyl nonafluorobutan-2-yl 5-312 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-313 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H H hexafluoropropan-2-yl 5-314 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H acetyl hexafluoropropan-2-yl 5-315 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H propanoyl hexafluoropropan-2-yl 5-316 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethoxy H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-317 chloro H 1,1,12,3,3,3- H chloro H H chloro H H tert-butoxy hepfluoropropan-2-yl carbonyl 5-318 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H chloro H H Cyclopropyl hexafluoropropan-2-yl carbonyl 5-319 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H chloro H H cyclopropylacetyl hexafluoropropan-2-yl 5-320 CH₃ H 1-bromo-1,1,2,3,3,3-- H ethyl H H chloro H H (methylsulfanyl) fluoropropan-2-yl acetyl 5-321 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H H nonafluorobutan-2-yl 5-322 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H acetyl nonafluorobutan-2-yl 5-323 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H propanoyl nonafluorobutan-2-yl 5-324 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-325 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H cyclopropylacetyl nonafluorobutan-2-yl 5-326 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H Cyclopropyl nonafluorobutan-2-yl carbonyl 5-327 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H (methylsulfanyl) nonafluorobutan-2-yl acetyl 5-328 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H tert-butoxy nonafluorobutan-2-yl carbonyl 5-329 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H tert-butoxy nonafluorobutan-2-yl carbonyl 5-330 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H cyclopropylacetyl nonafluorobutan-2-yl 5-331 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H chloro H H (methylsulfanyl) nonafluorobutan-2-yl acetyl 5-332 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H H heptafluoropropan-2-yl 5-333 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H acetyl heptafluoropropan-2-yl 5-334 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H propanoyl heptafluoropropan-2-yl 5-335 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-336 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H cyclopropylacetyl heptafluoropropan-2-yl 5-337 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H (methylsulfanyl) heptafluoropropan-2-yl acetyl 5-338 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H Cyclopropyl heptafluoropropan-2-yl carbonyl 5-339 CH₃ H 1,1,1,2,3,3,3- H chloro H H H H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-340 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H cyclopropylacetyl heptafluoropropan-2-yl 5-341 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H Cyclopropyl heptafluoropropan-2-yl carbonyl 5-342 CH₃ H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-343 chloro H 1,1,1,2,3,3,3- H chloro H H CH₃ H H H heptafluoropropan-2-yl 5-344 chloro H 1,1,1,2,3,3,3- H chloro H H CH₃ H H acetyl heptafluoropropan-2-yl 5-345 chloro H 1,1,1,2,3,3,3- H chloro H H CH₃ H H propanoyl heptafluoropropan-2-yl 5-346 chloro H 1,1,1,2,3,3,3- H chloro H H CH₃ H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-347 chloro H 1,1,1,2,3,3,3- H chloro H H CH₃ H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-348 chloro H 1,1,1,2,3,3,4,4,4- H chloro H H H H H trifluoroacetyl nonafluorobutan-2-yl 5-349 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H trifluoroacetyl heptafluoropropan-2-yl 5-350 chloro H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H H heptafluoropropan-2-yl sulfanyl 5-351 chloro H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H acetyl heptafluoropropan-2-yl sulfanyl 5-352 chloro H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H propanoyl heptafluoropropan-2-yl sulfanyl 5-353 chloro H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl sulfanyl propanoyl 5-354 chloro H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H H nonafluorobutan-2-yl sulfanyl 5-355 chloro H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H acetyl nonafluorobutan-2-yl sulfanyl 5-356 chloro H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H propanoyl nonafluorobutan-2-yl sulfanyl 5-357 chloro H 1,1,1,2,3,3,4,4,4- H (difluoromethyl)- H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl sulfanyl propanoyl 5-358 chloro H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H H hexafluoropropan-2-yl sulfanyl 5-359 chloro H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H acetyl hexafluoropropan-2-yl sulfanyl 5-360 chloro H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H propanoyl hexafluoropropan-2-yl sulfanyl 5-361 chloro H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl sulfanyl propanoyl 5-362 bromo H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H H heptafluoropropan-2-yl sulfanyl 5-363 bromo H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H acetyl heptafluoropropan-2-yl sulfanyl 5-364 bromo H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H propanoyl heptafluoropropan-2-yl sulfanyl 5-365 bromo H 1,1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl sulfanyl propanoyl 5-366 bromo H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H H hexafluoropropan-2-yl sulfanyl 5-367 bromo H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H acetyl hexafluoropropan-2-yl sulfanyl 5-368 bromo H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H propanoyl hexafluoropropan-2-yl sulfanyl 5-369 bromo H 1-bromo-1,1,2,3,3,3- H (difluoromethyl)- H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl sulfanyl propanoyl 5-370 chloro H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H H heptafluoropropan-2-yl sulfanyl 5-371 chloro H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H acetyl heptafluoropropan-2-yl sulfanyl 5-372 chloro H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H propanoyl heptafluoropropan-2-yl sulfanyl 5-373 chloro H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl sulfanyl propanoyl 5-374 chloro H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl) H H chloro H H H nonafluorobutan-2-yl sulfanyl 5-375 chloro H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl) H H chloro H H acetyl nonafluorobutan-2-yl sulfanyl 5-376 chloro H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl) H H chloro H H propanoyl nonafluorobutan-2-yl sulfanyl 5-377 chloro H 1,1,1,2,3,3,4,4,4- H (trifluoromethyl) H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl sulfanyl propanoyl 5-378 chloro H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H H hexafluoropropan-2-yl sulfanyl 5-379 chloro H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H acetyl hexafluoropropan-2-yl sulfanyl 5-380 chloro H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H propanoyl hexafluoropropan-2-yl sulfanyl 5-381 chloro H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl sulfanyl propanoyl 5-382 bromo H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H H heptafluoropropan-2-yl sulfanyl 5-383 bromo H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H acetyl heptafluoropropan-2-yl sulfanyl 5-384 bromo H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H propanoyl heptafluoropropan-2-yl sulfanyl 5-385 bromo H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl sulfanyl propanoyl 5-386 bromo H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H H hexafluoropropan-2-yl sulfanyl 5-387 bromo H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H acetyl hexafluoropropan-2-yl sulfanyl 5-388 bromo H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H propanoyl hexafluoropropan-2-yl sulfanyl 5-389 bromo H 1-bromo-1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl sulfanyl propanoyl 5-390 chloro H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H acetyl heptafluoropropan-2-yl sulfinyl 5-391 chloro H 1,1,1,2,3,3,3- H (trifluoromethyl) H H chloro H H acetyl heptafluoropropan-2-yl sulfonyl 5-392 chloro H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H H heptafluoropropan-2-yl 5-393 chloro H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H acetyl heptafluoropropan-2-yl 5-394 chloro H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H propanoyl heptafluoropropan-2-yl 5-395 chloro H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-396 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H H nonafluorobutan-2-yl 5-397 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H acetyl nonafluorobutan-2-yl 5-398 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H propanoyl nonafluorobutan-2-yl 5-399 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-400 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H H hexafluoropropan-2-yl 5-401 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H acetyl hexafluoropropan-2-yl 5-402 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H propanoyl hexafluoropropan-2-yl 5-403 chloro H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-404 bromo H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H H heptafluoropropan-2-yl 5-405 bromo H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H acetyl heptafluoropropan-2-yl 5-406 bromo H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H propanoyl heptafluoropropan-2-yl 5-407 bromo H 1,1,1,2,3,3,3- H difluoromethyl H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-408 bromo H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H H nonafluorobutan-2-yl 5-409 bromo H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H acetyl nonafluorobutan-2-yl 5-410 bromo H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H propanoyl nonafluorobutan-2-yl 5-411 bromo H 1,1,1,2,3,3,4,4,4- H difluoromethyl H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-412 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H H hexafluoropropan-2-yl 5-413 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H acetyl hexafluoropropan-2-yl 5-414 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H propanoyl hexafluoropropan-2-yl 5-415 bromo H 1-bromo-1,1,2,3,3,3- H difluoromethyl H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-416 chloro H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H H heptafluoropropan-2-yl 5-417 chloro H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H acetyl heptafluoropropan-2-yl 5-418 chloro H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H propanoyl heptafluoropropan-2-yl 5-419 chloro H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-420 chloro H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H H nonafluorobutan-2-yl 5-421 chloro H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H acetyl nonafluorobutan-2-yl 5-422 chloro H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H propanoyl nonafluorobutan-2-yl 5-423 chloro H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-424 chloro H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H H hexafluoropropan-2-yl 5-425 chloro H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H acetyl hexafluoropropan-2-yl 5-426 chloro H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H propanoyl hexafluoropropan-2-yl 5-427 chloro H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-428 bromo H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H H heptafluoropropan-2-yl 5-429 bromo H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H acetyl heptafluoropropan-2-yl 5-430 bromo H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H propanoyl heptafluoropropan-2-yl 5-431 bromo H 1,1,1,2,3,3,3- H trifluoromethyl H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-432 bromo H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H H nonafluorobutan-2-yl 5-433 bromo H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H acetyl nonafluorobutan-2-yl 5-434 bromo H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H propanoyl nonafluorobutan-2-yl 5-435 bromo H 1,1,1,2,3,3,4,4,4- H trifluoromethyl H H chloro H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-436 bromo H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H H hexafluoropropan-2-yl 5-437 bromo H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H acetyl hexafluoropropan-2-yl 5-438 bromo H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H propanoyl hexafluoropropan-2-yl 5-439 bromo H 1-bromo-1,1,2,3,3,3- H trifluoromethyl H H chloro H H 3,3,3-trifluoro- hexafluoropropan-2-yl propanoyl 5-440 bromo H 1,1,1,2,3,3,3- H bromo H H H H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-441 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H (2,2-difluorocyclo- heptafluoropropan-2-yl propyl)carbonyl 5-442 CH₃ H 1,1,1,2,3,3,3- H ethyl H H bromo H H cyanoacetyl heptafluoropropan-2-yl 5-443 CH3 H 1,1,1,2,3,3,3- H chloro H H chloro H H H heptafluoropropan-2-yl 5-444 CH3 H 1,1,1,2,3,3,3- H chloro H H chloro H H acetyl heptafluoropropan-2-yl 5-445 CH3 H 1,1,1,2,3,3,3- H chloro H H chloro H H propanoyl heptafluoropropan-2-yl 5-446 CH3 H 1,1,1,2,3,3,3- H chloro H H chloro H H 3,3,3-trifluoro- heptafluoropropan-2-yl propanoyl 5-447 CH3 H 1,1,1,2,3,3,3- H chloro H H chloro H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-448 chloro H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-449 bromo H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-450 chloro H 1,1,1,2,3,3,3- H difluoromethoxy H H chloro H H cyclopropylacetyl heptafluoropropan-2-yl 5-451 bromo H 1,1,1,2,3,3,3- H bromo H H chloro H H tert-butoxy heptafluoropropan-2-yl carbonyl 5-452 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H H H H 3,3,3-trifluoro- nonafluorobutan-2-yl propanoyl 5-453 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H H H H tert-butoxy nonafluorobutan-2-yl carbonyl 5-454 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H Cyclopropyl nonafluorobutan-2-yl carbonyl 5-455 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H cyclopropylacetyl nonafluorobutan-2-yl 5-456 chloro H 1,1,1,2,3,3,4,4,4- H difluoromethoxy H H chloro H H tert-butoxy nonafluorobutan-2-yl carbonyl

TABLE 6

Exa R1 R2 J R4 R5 Q R14 R15 6-1  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 6-2  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H acetyl 6-3  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H propanoyl 6-4  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H cyclopropylcarbonyl 6-5  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H cyclopropylacetyl 6-6  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H 3,3,3-trifluoropropanoyl 6-7  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H (2-fluoropyridin-3-yl)carbonyl 6-8  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H 6-9  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H acetyl 6-10 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H propanoyl 6-11 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H cyclopropylcarbonyl 6-12 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H cyclopropylacetyl 6-13 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H 3,3,3-trifluoropropanoyl 6-14 CH₃ H undecafluorocyclohexyl H ethyl H H H 6-15 CH₃ H undecafluorocyclohexyl H ethyl H H acetyl 6-16 CH₃ H undecafluorocyclohexyl H ethyl H H propanoyl 6-17 CH₃ H undecafluorocyclohexyl H ethyl H H cyclopropylcarbonyl 6-18 CH₃ H undecafluorocyclohexyl H ethyl H H cyclopropylacetyl 6-19 CH₃ H undecafluorocyclohexyl H ethyl H H 3,3,3-trifluoropropanoyl 6-20 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H 6-21 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H acetyl 6-22 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H propanoyl 6-23 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H 3,3,3-trifluoropropanoyl 6-24 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H 6-25 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H acetyl 6-26 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H propanoyl 6-27 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H 3,3,3-trifluoropropanoyl 6-28 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H 6-29 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H acetyl 6-30 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H propanoyl 6-31 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H 3,3,3-trifluoropropanoyl 6-32 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 6-33 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H acetyl 6-34 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H propanoyl 6-35 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-36 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H 6-37 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H acetyl 6-38 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H propanoyl 6-39 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H 3,3,3-trifluoropropanoyl 6-40 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 6-41 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H acetyl 6-42 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H propanoyl 6-43 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-44 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H 6-45 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H acetyl 6-46 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H propanoyl 6-47 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H 3,3,3-trifluoropropanoyl 6-48 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 6-49 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H acetyl 6-50 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H propanoyl 6-51 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-52 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 6-53 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H acetyl 6-54 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H propanoyl 6-55 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-56 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 6-57 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H acetyl 6-58 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H propanoyl 6-59 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-60 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 6-61 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H acetyl 6-62 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H propanoyl 6-63 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-64 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 6-65 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H acetyl 6-66 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H propanoyl 6-67 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-68 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 6-69 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H acetyl 6-70 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H propanoyl 6-71 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl 6-72 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 6-73 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H acetyl 6-74 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H propanoyl 6-75 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H 3,3,3-trifluoropropanoyl

TABLE 7

Exa R1 R2 J R4 R5 Q R8 R10 R14 R15 7-1  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H H 7-2  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H acetyl 7-3  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H propanoyl 7-4  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H cyclopropylcarbonyl 7-5  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H cyclopropylacetyl 7-6  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H 3,3,3-trifluoropropanoyl 7-7  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H H 7-8  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H acetyl 7-9  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H propanoyl 7-10  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H cyclopropylcarbonyl 7-11  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H cyclopropylacetyl 7-12  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H 3,3,3-trifluoropropanoyl 7-13  CH₃ H undecafluorocyclohexyl H ethyl H H H H H 7-14  CH₃ H undecafluorocyclohexyl H ethyl H H H H acetyl 7-15  CH₃ H undecafluorocyclohexyl H ethyl H H H H propanoyl 7-16  CH₃ H undecafluorocyclohexyl H ethyl H H H H cyclopropylcarbonyl 7-17  CH₃ H undecafluorocyclohexyl H ethyl H H H H cyclopropylacetyl 7-18  CH₃ H undecafluorocyclohexyl H ethyl H H H H 3,3,3-trifluoropropanoyl 7-19  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H tert-butoxycarbonyl 7-20  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H H H H 2-yl 7-21  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H H H acetyl 2-yl 7-22  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H H H propanoyl 2-yl 7-23  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H H H 3,3,3-trifluoropropanoyl 2-yl 7-24  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H H H H 2-yl 7-25  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H H H acetyl 2-yl 7-26  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H H H propanoyl 2-yl 7-27  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H H H 3,3,3-trifluoropropanoyl 2-yl 7-28  chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H chloro H H H H H 2-yl 7-29  chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H chloro H H H H acetyl 2-yl 7-30  chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H chloro H H H H propanoyl 2-yl 7-31  chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H chloro H H H H 3,3,3-trifluoropropanoyl 2-yl 7-32  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H bromo H H H H H 2-yl 7-33  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H bromo H H H H acetyl 2-yl 7-34  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H bromo H H H H propanoyl 2-yl 7-35  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H bromo H H H H 3,3,3-trifluoropropanoyl 2-yl 7-36  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H H 2-yl 7-37  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H acetyl 2-yl 7-38  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H propanoyl 2-yl 7-39  bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 2-yl 7-40  chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H chloro H H H H H 7-41  chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H chloro H H H H acetyl 7-42  chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H chloro H H H H propanoyl 7-43  chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H chloro H H H H 3,3,3-trifluoropropanoyl 7-44  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H H 7-45  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H acetyl 7-46  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H propanoyl 7-47  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H 3,3,3-trifluoropropanoyl 7-48  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H H 7-49  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H acetyl 7-50  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H propanoyl 7-51  bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 7-52  chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H chloro H H H H H 7-53  chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H chloro H H H H acetyl 7-54  chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H chloro H H H H propanoyl 7-55  chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H chloro H H H H 3,3,3-trifluoropropanoyl 7-56  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H H 7-57  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H acetyl 7-58  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H propanoyl 7-59  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H 3,3,3-trifluoropropanoyl 7-60  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H H 7-61  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H acetyl 7-62  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H propanoyl 7-63  bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 7-64  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H H 7-65  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H acetyl 7-66  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H propanoyl 7-67  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 7-68  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H H 7-69  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H acetyl 7-70  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H propanoyl 7-71  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 7-72  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H H 2-yl 7-73  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H acetyl 2-yl 7-74  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H propanoyl 2-yl 7-75  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 2-yl 7-76  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H chloro H H H 7-77  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H chloro H H acetyl 7-78  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H chloro H H propanoyl 7-79  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H chloro H H 3,3,3-trifluoropropanoyl 7-80  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H chloro H H H 7-81  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H chloro H H acetyl 7-82  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H chloro H H propanoyl 7-83  CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H chloro H H 3,3,3-trifluoropropanoyl 7-84  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H chloro H H H 7-85  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H chloro H H acetyl 7-86  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H chloro H H propanoyl 7-87  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H chloro H H 3,3,3-trifluoropropanoyl 7-88  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H chloro H H H 7-89  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H chloro H H acetyl 7-90  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H chloro H H propanoyl 7-91  CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H chloro H H 3,3,3-trifluoropropanoyl 7-92  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H chloro H H H 2-yl 7-93  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H chloro H H acetyl 2-yl 7-94  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H chloro H H propanoyl 2-yl 7-95  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H chloro H H 3,3,3-trifluoropropanoyl 2-yl 7-96  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H chloro H H H 2-yl 7-97  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H chloro H H acetyl 2-yl 7-98  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H chloro H H propanoyl 2-yl 7-99  CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H chloro H H 3,3,3-trifluoropropanoyl 2-yl 7-100 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H chloro H H 7-101 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H chloro H acetyl 7-102 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H chloro H propanoyl 7-103 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H CH₃ H H chloro H 3,3,3-trifluoropropanoyl 7-104 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H chloro H H 7-105 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H chloro H acetyl 7-106 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H chloro H propanoyl 7-107 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H chloro H 3,3,3-trifluoropropanoyl 7-108 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H chloro H H 7-109 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H chloro H acetyl 7-110 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H chloro H propanoyl 7-111 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H CH₃ H H chloro H 3,3,3-trifluoropropanoyl 7-112 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H chloro H H 7-113 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H chloro H acetyl 7-114 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H chloro H propanoyl 7-115 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H chloro H 3,3,3-trifluoropropanoyl 7-116 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H chloro H H 2-yl 7-117 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H chloro H acetyl 2-yl 7-118 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H CH₃ H H chloro H propanoyl 2-yl 7-119 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-l H CH₃ H H chloro H 3,3,3-trifluoropropanoyl 2-yl 7-120 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H chloro H H 2-yl 7-121 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H chloro H acetyl 2-yl 7-122 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H chloro H propanoyl 2-yl 7-123 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H ethyl H H chloro H 3,3,3-trifluoropropanoyl 2-yl 7-124 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H H 7-125 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H acetyl 7-126 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H propanoyl 7-127 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 7-128 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H H 7-129 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H acetyl 7-130 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H propanoyl 7-131 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoro-methoxy H H H H 3,3,3-trifluoropropanoyl 7-132 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H H 2-yl 7-133 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H acetyl 2-yl 7-134 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H propanoyl 2-yl 7-135 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan- H difluoromethoxy H H H H 3,3,3-trifluoropropanoyl 2-yl

TABLE 8

Exa R1 R2 J R4 R5 Q R7 R14 R15 8-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H 8-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H acetyl 8-3 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H propanoyl 8-4 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H cyclopropylcarbonyl 8-5 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H cyclopropylacetyl 8-6 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 8-7 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H 8-8 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H acetyl 8-9 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H propanoyl 8-10 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H cyclopropylcarbonyl 8-11 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H cyclopropylacetyl 8-12 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 8-13 CH₃ H undecafluorocyclohexyl H ethyl H H H H 8-14 CH₃ H undecafluorocyclohexyl H ethyl H H H acetyl 8-15 CH₃ H undecafluorocyclohexyl H ethyl H H H propanoyl 8-16 CH₃ H undecafluorocyclohexyl H ethyl H H H cyclopropylcarbonyl 8-17 CH₃ H undecafluorocyclohexyl H ethyl H H H cyclopropylacetyl 8-18 CH₃ H undecafluorocyclohexyl H ethyl H H H 3,3,3-trifluoropropanoyl 8-19 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H tert-butoxycarbonyl 8-20 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH3 H H H H 8-21 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH3 H H H acetyl 8-22 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH3 H H H propanoyl 8-23 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH3 H H H 3,3,3-trifluoropropanoyl 8-24 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H H 8-25 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H acetyl 8-26 CH3 H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H propanoyl 8-27 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 8-28 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H H 8-29 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H acetyl 8-30 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H propanoyl 8-31 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 8-32 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 8-33 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 8-34 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 8-35 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-36 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H 8-37 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H acetyl 8-38 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H propanoyl 8-39 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 8-40 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 8-41 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 8-42 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 8-43 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-44 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H 8-45 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H acetyl 8-46 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H propanoyl 8-47 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 8-48 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 8-49 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 8-50 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 8-51 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-52 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 8-53 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 8-54 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 8-55 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-56 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 8-57 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 8-58 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 8-59 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-60 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 8-61 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 8-62 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 8-63 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-64 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 8-65 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 8-66 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 8-67 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-68 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 8-69 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 8-70 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 8-71 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 8-72 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 8-73 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 8-74 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 8-75 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl

TABLE 9

Exa R1 R2 J R4 R5 Q R8 R12 R13 R14 R15 9-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H H 9-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H acetyl 9-3 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H propanoyl 9-4 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H cyclopropylcarbonyl 9-5 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H cyclopropylacetyl 9-6 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H 3,3,3-trifluoropropanoyl 9-7 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H CH₃ H H tert-butoxycarbonyl 9-8 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H H 9-9 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H acetyl 9-10 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H propanoyl 9-11 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H cyclopropylcarbonyl 9-12 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H cyclopropylacetyl 9-13 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H 3,3,3-trifluoropropanoyl 9-14 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H CH₃ H H tert-butoxycarbonyl 9-15 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H H 9-16 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H acetyl 9-17 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H propanoyl 9-18 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H cyclopropylcarbonyl 9-19 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H cyclopropylacetyl 9-20 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H 3,3,3-trifluoropropanoyl 9-21 CH₃ H undecafluorocyclohexyl H ethyl H H CH₃ H H tert-butoxycarbonyl 9-22 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H CH₃ H H H 9-23 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H CH₃ H H acetyl 9-24 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H CH₃ H H propanoyl 9-25 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H CH₃ H H 3,3,3-trifluoropropanoyl 9-26 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H CH₃ H H H 9-27 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H CH₃ H H acetyl 9-28 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H CH₃ H H propanoyl 9-29 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H CH₃ H H 3,3,3-trifluoropropanoyl 9-30 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H CH₃ H H H 9-31 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H CH₃ H H acetyl 9-32 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H CH₃ H H propanoyl 9-33 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H CH₃ H H 3,3,3-trifluoropropanoyl 9-34 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H H 9-35 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-36 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-37 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-38 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H CH₃ H H H 9-39 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H CH₃ H H acetyl 9-40 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H CH₃ H H propanoyl 9-41 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H CH₃ H H 3,3,3-trifluoropropanoyl 9-42 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H H 9-43 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-44 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-45 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-46 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H CH₃ H H H 9-47 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H CH₃ H H acetyl 9-48 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H CH₃ H H propanoyl 9-49 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H CH₃ H H 3,3,3-trifluoropropanoyl 9-50 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H H 9-51 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-52 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-53 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-54 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H H 9-55 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-56 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-57 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-58 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H H 9-59 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-60 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-61 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-62 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H H 9-63 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-64 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-65 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-66 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H H 9-67 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-68 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-69 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-70 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H H 9-71 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-72 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-73 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl 9-74 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H H 9-75 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H acetyl 9-76 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H propanoyl 9-77 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H CH₃ H H 3,3,3-trifluoropropanoyl

TABLE 10

Exa R1 R2 J R4 R5 Q R7 R14 R15 10-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H 10-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H acetyl 10-3 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H propanoyl 10-4 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H cyclopropylcarbonyl 10-5 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H cyclopropylacetyl 10-6 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 10-7 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H tert-butoxycarbonyl 10-8 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H 10-9 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H acetyl 10-10 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H propanoyl 10-11 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H cyclopropylcarbonyl 10-12 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H cyclopropylacetyl 10-13 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 10-14 CH₃ H undecafluorocyclohexyl H ethyl H H H tert-butoxycarbonyl 10-15 CH₃ H undecafluorocyclohexyl H ethyl H H H H 10-16 CH₃ H undecafluorocyclohexyl H ethyl H H H acetyl 10-17 CH₃ H undecafluorocyclohexyl H ethyl H H H propanoyl 10-18 CH₃ H undecafluorocyclohexyl H ethyl H H H cyclopropylcarbonyl 10-19 CH₃ H undecafluorocyclohexyl H ethyl H H H cyclopropylacetyl 10-20 CH₃ H undecafluorocyclohexyl H ethyl H H H 3,3,3-trifluoropropanoyl 10-21 CH₃ H undecafluorocyclohexyl H ethyl H H H tert-butoxycarbonyl 10-22 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H (methylsulfanyl)acetyl 10-23 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H H 10-24 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H acetyl 10-25 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H propanoyl 10-26 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H 3,3,3-trifluoropropanoyl 10-27 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H H 10-28 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H acetyl 10-29 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H propanoyl 10-30 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 10-31 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H H 10-32 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H acetyl 10-33 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H propanoyl 10-34 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 10-35 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 10-36 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 10-37 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 10-38 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-39 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H 10-40 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H acetyl 10-41 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H propanoyl 10-42 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 10-43 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 10-44 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 10-45 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 10-46 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-47 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H 10-48 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H acetyl 10-49 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H propanoyl 10-50 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 10-51 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 10-52 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 10-53 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 10-54 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-55 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 10-56 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 10-57 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 10-58 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-59 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 10-60 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 10-61 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 10-62 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-63 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 10-64 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 10-65 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 10-66 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-67 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 10-68 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 10-69 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 10-70 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-71 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 10-72 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 10-73 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 10-74 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 10-75 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 10-76 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 10-77 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 10-78 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl

TABLE 11

Exa R1 R2 J R4 R5 Q R7 R14 R15 11-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H H 11-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H acetyl 11-3 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H propanoyl 11-4 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H cyclopropylcarbonyl 11-5 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H cyclopropylacetyl 11-6 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 11-7 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H H tert-butoxycarbonyl 11-8 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H H 11-9 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H acetyl 11-10 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H propanoyl 11-11 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H cyclopropylcarbonyl 11-12 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H cyclopropylacetyl 11-13 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 11-14 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H ethyl H H H tert-butoxycarbonyl 11-15 CH₃ H undecafluorocyclohexyl H ethyl H H H H 11-16 CH₃ H undecafluorocyclohexyl H ethyl H H H acetyl 11-17 CH₃ H undecafluorocyclohexyl H ethyl H H H propanoyl 11-18 CH₃ H undecafluorocyclohexyl H ethyl H H H cyclopropylcarbonyl 11-19 CH₃ H undecafluorocyclohexyl H ethyl H H H cyclopropylacetyl 11-20 CH₃ H undecafluorocyclohexyl H ethyl H H H 3,3,3-trifluoropropanoyl 11-21 CH₃ H undecafluorocyclohexyl H ethyl H H H tert-butoxycarbonyl 11-22 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H H 11-23 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H acetyl 11-24 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H propanoyl 11-25 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H CH₃ H H H 3,3,3-trifluoropropanoyl 11-26 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H H 11-27 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H acetyl 11-28 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H propanoyl 11-29 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H ethyl H H H 3,3,3-trifluoropropanoyl 11-30 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H H 11-31 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H acetyl 11-32 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H propanoyl 11-33 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 11-34 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 11-35 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 11-36 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 11-37 bromo H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-38 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H H 11-39 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H acetyl 11-40 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H propanoyl 11-41 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 11-42 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 11-43 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 11-44 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 11-45 bromo H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-46 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H H 11-47 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H acetyl 11-48 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H propanoyl 11-49 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H bromo H H H 3,3,3-trifluoropropanoyl 11-50 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 11-51 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 11-52 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 11-53 bromo H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-54 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 11-55 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 11-56 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 11-57 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-58 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 11-59 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 11-60 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 11-61 CH₃ H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-62 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 11-63 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 11-64 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 11-65 CH₃ H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-66 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H H 11-67 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H acetyl 11-68 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H propanoyl 11-69 chloro H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-70 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H H 11-71 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H acetyl 11-72 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H propanoyl 11-73 chloro H 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl 11-74 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H H 11-75 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H acetyl 11-76 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H propanoyl 11-77 chloro H 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl H difluoromethoxy H H H 3,3,3-trifluoropropanoyl

TABLE 12

Exa R1 R2 J R4 R5 Q R7 R12 R13 R14 R15 W 12-1 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H tert-butoxycarbonyl 1H-1,2,4-triazol-1-yl heptafluoropropan-2-yl 12-2 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H H 1H-1,2,4-triazol-1-yl heptafluoropropan-2-yl 12-3 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H acetyl 1H-1,2,4-triazol-1-yl heptafluoropropan-2-yl 12-4 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H propionyl 1H-1,2,4-triazol-1-yl heptafluoropropan-2-yl 12-5 CH₃ H 1,1,1,2,3,3,3- H ethyl H H H H H methoxycarbonyl 1H-1,2,4-triazol-1-yl heptafluoropropan-2-yl 12-6 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H tert-butoxycarbonyl 1H-1,2,4-triazol-1-yl nonafluorobutan-2-yl 12-7 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H H 1H-1,2,4-triazol-1-yl nonafluorobutan-2-yl 12-8 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H acetyl 1H-1,2,4-triazol-1-yl nonafluorobutan-2-yl 12-9 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H propionyl 1H-1,2,4-triazol-1-yl nonafluorobutan-2-yl 12-10 CH₃ H 1,1,1,2,3,3,4,4,4- H ethyl H H H H H methoxycarbonyl 1H-1,2,4-triazol-1-yl nonafluorobutan-2-yl 12-11 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H H H H tert-butoxycarbonyl 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl 12-12 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H H H H H 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl 12-13 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H H H H acetyl 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl 12-14 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H H H H propionyl 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl 12-15 CH₃ H 1-bromo-1,1,2,3,3,3- H ethyl H H H H H methoxycarbonyl 1H-1,2,4-triazol-1-yl hexafluoropropan-2-yl

TABLE 13

Exa R1 R2 J R4 R5 Q R7 W R9 R10 R12 R13 R14 R15 13-1 CH₃ H 1,1,1,2,3,3,3- H ethyl H H 1H-pyrazol-1-yl H H H H H propanoyl heptafluoropropan-2-yl 13-2 CH₃ H 1,1,1,2,3,3,3- H ethyl H H 1H-1,2,4-triazol-1-yl H H H H H acetyl heptafluoropropan-2-yl 13-3 CH₃ H 1,1,1,2,3,3,3- H ethyl H H 1H-1,2,4-triazol-1-yl H H H H H propanoyl heptafluoropropan-2-yl

TABLE 14

Exa R1 R2 J R4 R5 Q R7 W R11 14-1 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H 1H-pyrazol-1-yl cyano 14-2 CH₃ H 1,1,1,2,3,3,3-heptafluoropropan-2-yl H ethyl H H 1H-1,2,4-triazol-1-yl cyano

TABLE A

Exa X¹⁶ J X¹⁷ X¹⁴ X¹³ A-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl CH₃ trifluoromethyl fluoro A-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl fluoro fluoro A-3 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl CH₃ chloro fluoro A-4 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl bromo fluoro A-5 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl trifluoromethyl fluoro A-6 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H iodo A-7 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro chloro iodo A-8 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo H iodo A-9 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro CH₃ iodo A-10 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro chloro iodo A-11 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro chloro iodo

TABLE B

Exa X¹⁶ J X¹⁷ X¹⁵ X¹³ B-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan- CH₃ chloro fluoro 2-yl B-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan- CH₃ trifluoro- fluoro 2-yl methyl B-3 CH₃ 1,1,1,2,3,3,3-heptafluoropropan- CH₃ nitro fluoro 2-yl

TABLE C

Exa X¹⁶ J X¹⁷ X¹³ C-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl CH₃ chloro C-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl chloro C-3 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl chloro C-4 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl chloro

TABLE D

Exa X¹⁶ J X¹⁷ X¹³ D-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl bromo D-2 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl CH₃ bromo D-3 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl bromo D-4 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl CH₃ bromo D-5 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl bromo

TABLE E

Exa X¹⁶ J X¹⁷ X¹³ E-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl fluoro

TABLE F

Exa X¹⁶ J X¹⁷ X¹⁹ X¹⁸ F-1 CH₃ 1,1,1,2,3,3,3- CH₃ H chloro heptafluoropropan-2-yl F-2 CH₃ 1,1,1,2,3,3,3- CH₃ H 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl F-3 CH₃ 1,1,1,2,3,3,3- ethyl H chloro heptafluoropropan-2-yl F-4 CH₃ 1,1,1,2,3,3,3- ethyl H 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl F-5 CH₃ 1,1,1,2,3,3,3- ethyl chloro chloro heptafluoropropan-2-yl F-6 CH₃ 1,1,1,2,3,3,3- ethyl chloro 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl F-7 CH₃ 1,1,1,2,3,3,3- ethyl bromo chloro heptafluoropropan-2-yl F-8 CH₃ 1,1,1,2,3,3,3- ethyl bromo 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl F-9 CH₃ 1,1,1,2,3,3,3- ethyl nitro 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl F-10 CH₃ 1,1,1,2,3,3,4,4,4- ethyl H chloro nonafluorobutan-2-yl F-11 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl H 1,3-dioxo-1,3-dihydro- F-12 CH₃ 1,1,1,2,3,3,4,4,4- ethyl fluoro chloro nonafluorobutan-2-yl F-13 CH₃ 1,1,1,2,3,3,4,4,4- ethyl fluoro 1,3-dioxo-1,3-dihydro- nonafluorobutan-2-yl 2H-isoindol-2-yl F-14 CH₃ 1,1,1,2,3,3,4,4,4- ethyl chloro chloro nonafluorobutan-2-yl F-15 CH₃ 1,1,1,2,3,3,4,4,4- ethyl chloro 1,3-dioxo-1,3-dihydro- nonafluorobutan-2-yl 2H-isoindol-2-yl F-16 CH₃ 1,1,1,2,3,3,4,4,4- ethyl bromo 1,3-dioxo-1,3-dihydro- nonafluorobutan-2-yl 2H-isoindol-2-yl F-17 CH₃ 1,1,1,2,3,3,3- ethyl iodo 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl F-18 CH₃ 1-bromo-1,1,2,3,3,3- ethyl chloro chloro hexafluoropropan-2-yl F-19 CH₃ 1-bromo-1,1,2,3,3,3- ethyl chloro 1,3-dioxo-1,3-dihydro- hexafluoropropan-2-yl 2H-isoindol-2-yl

TABLE G

Exa X¹⁶ J X¹⁷ X¹⁸ G-1 CH₃ 1,1,1,2,3,3,3- ethyl chloro heptafluoropropan-2-yl G-2 CH₃ 1,1,1,2,3,3,3- ethyl 1,3-dioxo-1,3-dihydro- heptafluoropropan-2-yl 2H-isoindol-2-yl G-3 CH₃ 1,1,1,2,3,3,4,4,4- ethyl chloro nonafluorobutan-2-yl G-4 CH₃ 1,1,1,2,3,3,4,4,4- ethyl 1,3-dioxo-1,3-dihydro- nonafluorobutan-2-yl 2H-isoindol-2-yl G-5 CH₃ 1-bromo-1,1,2,3,3,3- ethyl chloro hexafluoropropan-2-yl G-6 CH₃ 1-bromo-1,1,2,3,3,3- ethyl 1,3-dioxo-1,3-dihydro- hexafluoropropan-2-yl 2H-isoindol-2-yl

TABLE H

Exa X¹⁶ J X¹⁷ X²⁰ X²¹ H-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl CH₃ O H-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl CH₃ N(OH) H-3 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl CH₃ O H-4 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl CH₃ N(OH) H-5 CH₃ 1-bromo-1,1,2,3,3,3- ethyl CH₃ O hexafluoropropan-2-yl H-6 CH₃ 1-bromo-1,1,2,3,3,3- ethyl CH₃ N(OH) hexafluoropropan-2-yl

TABLE I

Exa X¹⁶ J X¹⁷ X²⁴ X²³ I-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl CH₃ fluoro H I-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl H H I-3 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl fluoro H I-4 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl chloro H I-5 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl H methyl I-6 CH₃ 1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl ethyl H H I-7 CH₃ 1,1,1,3,3,3-hexafluoro-2-[(methylsulfonyl)oxy] ethyl H H propan-2-yl I-8 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl H H I-9 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl H H I-10 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl H H I-11 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl H H I-12 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl difluoromethoxy chloro H I-13 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl difluoromethoxy chloro H I-14 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl difluoromethoxy chloro H I-15 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl difluoromethoxy chloro H I-16 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl difluoromethoxy chloro H I-17 chloro 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl difluoromethoxy chloro H I-18 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl difluoromethoxy chloro H I-19 bromo 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl difluoromethoxy chloro H I-20 bromo 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl difluoromethoxy chloro H I-21 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl CH₃ chloro H I-22 chloro 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl chloro chloro H I-23 bromo 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl bromo chloro H I-24 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H H I-25 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro CH₃ H I-26 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo H H I-27 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro H H I-28 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H H I-29 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl CH₃ fluoro H I-30 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl fluoro H I-31 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl fluoro H I-32 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro chloro H I-33 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo H H I-34 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo chloro H I-35 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro chloro H I-36 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl chloro H I-37 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo chloro H I-38 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro chloro H

TABLE J

Exa X¹⁶ J X¹⁷ J-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl J-2 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl J-3 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl

TABLE K

Exa X¹⁶ J X¹⁷ K-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl K-2 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl CH₃ K-3 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl K-4 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl CH₃ K-5 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl

TABLE L

Exa X¹⁶ J X¹⁷ X²¹ L-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl O L-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl N(OH) L-3 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl O L-4 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl N(OH) L-5 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl O L-6 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl N(OH)

TABLE M

Exa X¹⁶ J X¹⁷ X²¹ M-1 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl O M-2 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl N(OH) M-3 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl O M-4 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl N(OH) M-5 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl O M-6 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl N(OH)

TABLE N

Exa X¹⁶ J X¹⁷ X²⁶ N-1 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H N-2 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro H N-3 chloro 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl chloro H N-4 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro CH₃ N-5 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro CH₃ N-6 chloro 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl chloro CH₃ N-7 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H N-8 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro H N-9 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl chloro H N-10 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl H N-11 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl H N-12 CH₃ 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl ethyl H N-13 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo H N-14 bromo 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl bromo H N-15 bromo 1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl bromo H

TABLE O

Exa X¹⁶ J X¹⁷ X²⁶ O-1 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H O-2 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro H O-3 chloro 1-bromo-1,1,2,3,3,3- chloro H hexafluoropropan-2-yl O-4 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro chloro O-5 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro chloro O-6 chloro 1-bromo-1,1,2,3,3,3- chloro chloro hexafluoropropan-2-yl O-7 chloro 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro CH₃ O-8 chloro 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro CH₃ O-9 chloro 1-bromo-1,1,2,3,3,3- chloro CH₃ hexafluoropropan-2-yl O-10 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro H O-11 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro H O-12 CH₃ 1-bromo-1,1,2,3,3,3- chloro H hexafluoropropan-2-yl O-13 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl H O-14 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl H O-15 CH₃ 1-bromo-1,1,2,3,3,3- ethyl H hexafluoropropan-2-yl O-16 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl chloro O-17 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl chloro O-18 CH₃ 1-bromo-1,1,2,3,3,3- ethyl chloro hexafluoropropan-2-yl O-19 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl ethyl bromo O-20 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl ethyl bromo O-21 CH₃ 1-bromo-1,1,2,3,3,3- ethyl bromo hexafluoropropan-2-yl O-22 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo H O-23 bromo 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl bromo H O-24 bromo 1-bromo-1,1,2,3,3,3- bromo H hexafluoropropan-2-yl O-25 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo chloro O-26 bromo 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl bromo chloro O-27 bromo 1-bromo-1,1,2,3,3,3- bromo chloro hexafluoropropan-2-yl O-28 bromo 1,1,1,2,3,3,3-heptafluoropropan-2-yl bromo bromo O-29 bromo 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl bromo bromo O-30 bromo 1-bromo-1,1,2,3,3,3- bromo bromo hexafluoropropan-2-yl O-31 CH₃ 1,1,1,2,3,3,3-heptafluoropropan-2-yl chloro chloro O-32 CH₃ 1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl chloro chloro O-33 CH₃ 1-bromo-1,1,2,3,3,3- chloro chloro hexafluoropropan-2-yl

NMR Table Exa NMR 1-1 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 6.53 (1H, dd), 7.36 (2H, s), 7.57 (1H, s), 7.77 (1H, s), 7.84 (2H, d), 8.02-8.00 (3H, m). 1-2 ¹H-NMR (CDCl₃) δ: 2.36 (6H, s), 7.37 (2H, s), 7.41 (1H, s), 7.70 (1H, s), 7.81 (2H, d), 8.01 (1H, s), 8.03 (2H, d). 1-3 ¹H-NMR (CDCl₃) δ: 2.37 (6H, s), 7.38 (2H, s), 7.46 (1H, s), 7.88 (2H, d), 8.09 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-4 ¹H-NMR (CDCl₃) δ: 2.30 (6H, s), 3.35 (3H, s), 7.26 (3H, s), 7.39 (2H, d), 7.49 (2H, d), 8.07 (1H, s), 8.49 (1H, s). 1-5 ¹H-NMR (CDCl₃) δ: 2.42 (6H, s), 7.39 (2H, s), 7.68 (1H, s), 7.75 (1H, dd), 7.93 (1H, d), 8.02 (1H, d), 8.16 (1H, s), 8.65 (1H, s). 1-6 ¹H-NMR (CDCl₃) δ: 2.42 (6H, s), 7.18 (1H, s), 7.38 (2H, s), 7.90 (1H, d), 8.02 (1H, dd), 8.17-8.18 (2H, m), 8.70 (1H, s). 1-7 ¹H-NMR (DMSO-d₆) δ: 2.40 (6H, s), 7.45 (2H, s), 7.95 (1H, s), 8.07 (1H, d), 8.38 (1H, s), 8.39 (1H, dd), 8.65 (1H, d), 9.57 (1H, s). 1-8 ¹H-NMR (CDCl₃) δ: 2.36 (6H, s), 7.38 (2H, s), 7.51 (1H, s), 7.81 (1H, d), 7.96 (1H, dd), 8.16 (1H, d), 8.18 (1H, s), 8.70 (1H, s). 1-9 ¹H-NMR (CDCl₃) δ: 2.34 (6H, s), 7.38 (2H, s), 7.69-7.71 (2H, m), 8.01 (1H, dd), 8.17 (1H, s), 8.34 (1H, d), 8.63 (1H, s). 1-10 ¹H-NMR (CDCl₃) δ: 2.37 (6H, s), 7.39 (2H, s), 7.59 (1H, s), 7.75 (1H, d), 8.19 (1H, s), 8.27 (1H, d), 8.41 (2H, s). 1-11 ¹H-NMR (CDCl₃) δ: 2.35 (6H, s), 7.39 (2H, s), 7.79 (1H, d), 7.84 (1H, s), 8.15 (1H, s), 8.34 (1H, dd), 8.48 (1H, s), 8.55 (1H, d). 1-12 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 7.38 (2H, s), 7.88 (1H, s), 7.98 (1H, d), 8.20 (1H, s), 8.33 (1H, dd), 8.44 (1H, d), 8.91 (1H, s). 1-13 ¹H-NMR (CDCl₃) δ: 1.52 (3H, t), 2.36 (6H, s), 3.46 (2H, q), 7.38 (2H, s), 7.64 (1H, s), 7.78 (2H, d), 8.13 (2H, d). 1-14 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 6.42 (2H, d), 6.83 (2H, d), 7.39 (2H, s), 7.47-7.63 (2H, m), 8.24 (1H, m), 8.40 (1H, s) 1-15 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 6.41-6.43 (1H, m), 7.04-7.05 (2H, m), 7.40 (2H, s), 7.62 (1H, d), 7.78 (1H, s), 8.24 (1H, dd), 8.40 (1H, d). 1-16 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 6.54 (1H, dd), 7.38 (2H, s), 7.42 (1H, s), 7.78 (1H, d), 7.87 (2H, d), 8.04-8.01 (3H, m). 1-17 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 6.56 (1H, d), 7.39 (2H, s), 7.69-7.75 (4H, m), 8.24 (1H, d), 8.37 (1H, d). 1-18 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.38 (3H, s), 2.74 (2H, q), 6.60 (1H, t), 7.40 (2H, m), 7.56 (4H, tt), 7.92-8.03 (6H, m), 9.42 (1H, d), 11.92 (1H, s). 1-19 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.38 (3H, s), 2.69 (2H, q), 6.56-6.59 (1H, m), 7.14-7.34 (2H, m), 7.39 (2H, tt), 7.49-7.57 (2H, m), 7.71-7.77 (1H, m), 7.85-7.95 (3H, m), 8.06 (1H, t), 9.33 (1H, s), 11.44-11.51 (1H, d). 1-20 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.39 (3H, s), 2.70 (2H, q), 3.454 (1H, d), 3.74 (1H, d), 6.58 (1H, d), 7.40 (3, m), 7.57 (1H, d), 7.72-7.83 (2H, m), 7.92-8.08 (3H, m), 8.54 (1H, d), 9.35 (1H, s), 11.63 (1H, s). 1-21 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 7.38 (2H, s), 7.41 (1H, s), 7.70 (1H, s), 7.81 (2H, d), 8.01 (1H, s), 8.03 (2H, d). 1-22 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 7.40 (2H, s), 7.76 (1H, s), 7.95 (1H, s), 8.02 (1H, s), 8.10 (2H, s), 8.33 (1H, dd), 8.51 (1H, d). 1-23 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 7.41 (2H, s), 7.61 (1H, s), 7.80 (1H, d), 8.31 (1H, s), 8.34 (1H, dd), 8.54 (1H, d), 8.54 (1H, s). 1-24 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 7.41 (2H, s), 7.65 (1H, s), 7.77 (1H, d), 8.04 (1H, s), 8.23 (1H, s), 8.33 (1H, dd), 8.51 (1H, d). 1-25 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.71 (2H, q), 7.24 (1H, s), 7.36 (1H, s), 7.39 (2H, s), 7.54 (2H, d), 7.78 (1H, s), 7.92 (1H, s), 8.07 (2H, d). 1-26 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.70 (2H, q), 7.11 (1H, d, J), 7.20 (1H, d), 7.42 (2H, s), 7.63-7.67 (2H, m), 8.36 (2H, m), 8.60 (1H, d). 1-27 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 7.39 (2H, s), 7.63 (1H, s), 7.89-7.94 (3H, m), 8.13-8.10 (3H, m). 1-28 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.33 (3H, s), 2.70 (2H, q), 7.22-7.32 (2H, m), 7.75-7.84 (3H, m), 7.89-7.96 (2H, m), 8.34-8.38 (2H, m), 8.59 (1H, s). 1-29 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 7.39 (2H, s), 7.46 (1H, s), 7.88 (2H, s), 8.05 (2H, d), 8.25 (2H, d). 1-30 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.70 (2H, q), 7.41 (2H, s), 7.83 (2H, d), 7.94 (2H, d), 8.20 (1H, dd), 8.32 (1H, s). 1-31 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.39 (2H, s), 7.44 (1H, s), 7.88 (2H, d), 8.09 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-32 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.34 (3H, s), 2.37 (3H, s), 2.70 (2H, q), 7.39 (2H, s), 7.48 (1H, d), 7.62 (1H, s), 7.86 (1H, d), 7.95 (1H, s), 8.16 (1H, s), 8.33 (1H, s). 1-33 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.41 (2H, s), 7.63 (1H, s), 7.75 (1H, d), 8.19 (1H, s), 8.27 (1H, dd), 8.39-8.43 (2H, m). 1-34 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.70 (2H, q), 7.40 (2H, s), 7.50 (1H, s), 7.85 (1H, d), 7.92 (1H, d), 8.17-8.12 (2H, m), 8.80 (1H, d). 1-35 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.35 (3H, s), 2.69 (2H, q), 7.39 (2H, s), 7.57 (1H, s), 7.80 (1H, d), 7.95 (1H, dd), 8.16-8.17 (2H, m), 8.70 (1H, s). 1-36 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 7.40 (2H, s), 7.53 (1H, s), 7.71 (1H, d), 8.00 (1H, dd), 8.18 (1H, s), 8.33 (1H, d), 8.64 (1H, s). 1-37 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 4.04 (3H, s), 7.37 (2H, s), 7.56-7.53 (2H, m), 7.75 (1H, s), 8.01 (1H, d), 8.09 (1H, s), 8.91 (1H, s). 1-38 ¹H-NMR (DMSO-d₆) δ: 1.25 (3H, t),, 2.31 (3H, s), 2.70 (2H, q), 5.75 (2H, s), 7.28 (1H, dd), 7.37-7.49 (4H, m), 8.29 (1H, s), 8.95 (1H, s), 9.92 (1H, s). 1-39 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.69 (H, q), 7.40 (2H, s), 7.79 (1H, dd), 7.91 (1H, s), 8.15 (1H, s), 8.34 (1H, dd), 8.48 (1H, s), 8.56 (1H, s). 1-40 ¹H-NMR (CDCl₃) δ: 1.08-1.35 (6H, m), 2.37 (3H, s), 2.46 (2H, q), 2.71 (2H, q), 7.39 (1H, d), 7.55 (1H, s), 7.87 (1H, dd), 8.29 (1H, s), 8.57 (1H, s), 9.15 (1H, s), 9.97 (1H, s). 1-41 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.38 (3H, s), 2.70-2.78 (2H, q), 7.42 (2H, s), 7.51-7.65 (4H, m), 7.91-8.01 (4H, m), 8.36 (1H, s), 8.63 (1H, s), 9.37 (1H, s), 10.95 (1H, s). 1-42 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.40 (3H, s), 2.70-2.78 (2H, q),, 7.19-7.38 (2H, m), 7.40 (2H, s), 7.51-7.62 (2H, m), 7.97 (2H, dd), 8.05-8.11 (1H, m), 8.30 (1H, s), 8.56 (1H, s), 9.28 (1H, s), 10.60 (1H, d). 1-43 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.39 (3H, s), 2.74 (2H, q), 7.09-7.26 (2H, m), 7.39 (2H, s), 7.63 (1H, d), 7.94-8.04 (3H, m), 8.04-8.11 (1H, m), 8.36 (1H, s), 8.65 (1H, s,), 9.32 (1H, s), 10.97 (1H, s). 1-44 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.39 (3H, s), 2.71-2.78 (2H, q), 7.14-7.33 (2H, m), 7.40 (2H, s), 7.58-7.65 (1H, m), 7.79 (1H, s), 7.88 (1H, d), 7.98 (1H, dd), 8.30 (1H, s), 8.56 (1H, s), 9.24 (1H, d), 10.67-10.73 (1H, d). 1-45 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.39 (3H, s), 2.71-2.78 (2H, q), 7.43 (3H, m), 7.61 (1H, d), 7.83 (1H, s), 7.97 (1H, d), 8.34 (1H, s), 8.42 (1H, dd), 8.59 (2H, m), 9.26 (1H, s), 10.96 (1H, d). 1-46 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.41 (3H, s), 2.75 (2H, q), 7.40-7.45 (3H, m), 7.62 (1H, d), 7.86 (1H, s), 8.03 (1H, dd), 8.24 (1H, s), 8.55-8.60 (2H, m), 9.28 (1H, s), 10.65 (1H, s). 1-47 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 3.79 (3H, s), 7.38 (2H, s), 7.51 (1H, d), 7.79-7.84 (2H, m), 8.26 (1H, s), 8.54 (1H, s), 8.91 (1H, s), 9.30 (1H, s). 1-48 ¹H-NMR (acetone-d₆) δ: 1.21 (3H, t), 2.39 (3H, s), 2.79 (2H, q), 3.05 (3H, s), 7.48 (2H, s), 7.91 (1H, d), 8.04 (1H, dd), 8.31 (1H, s), 8.42 (1H, d), 9.03 (1H, s), 9.18 (1H, s), 9.48 (1H, s). 1-49 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.35 (3H, s), 2.68 (2H, q), 7.41 (2H, s), 7.59 (1H, s), 8.01 (1H, d), 8.22 (1H, s), 8.31 (1H, dd), 8.42 (1H, d), 8.92 (1H, s). 1-50 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.40 (2H, s), 7.46 (1H, s), 7.90 (2H, d), 8.12 (2H, d), 8.73 (1H, s). 1-52 ¹H-NMR (CDCl₃) δ: 1.23 (3H, td, J = 7.4, 4.9 Hz), 2.34 (3H, s), 2.69 (2H, q, J = 7.6 Hz), 7.40 (2H, s), 7.81 (1H, d, J = 8.2 Hz), 8.15 (1H, s), 8.41 (1H, dd, J = 8.2, 1.9 Hz), 8.54 (1H, s), 8.70 (1H, d, J = 1.8 Hz). 1-53 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.69 (2H, q), 3.99 (3H, s), 7.39 (2H, s), 7.78 (1H, d), 8.45 (1H, dd), 8.50 (1H, s), 8.74 (1H, d), 8.77 (1H, s). 1-54 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 5.83 (1H, s), 7.10 (1H, s), 7.39 (2H, s), 7.58 (1H, s), 7.94 (2H, d), 8.12 (2H, d), 8.69 (1H, s). 1-55 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.40 (2H, s), 7.63 (1H, s), 7.91 (2H, d), 8.17 (2H, d), 9.11 (1H, s). 1-56 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.38 (3H, s), 2.73 (2H, q), 7.40 (2H, s), 7.70-7.82 (2H, m), 8.00 (1H, d), 8.44 (1H, dd), 9.13 (1H, s). 1-57 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.69 (2H, q), 7.42 (2H, s), 7.47 (1H, s,), 7.79 (1H, d), 8.31 (1H, dd), 8.85 (1H, d), 9.64 (1H, d). 1-58 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.72 (2H, q), 7.40 (2H, s), 7.48 (1H, s), 8.14 (2H, d), 8.34 (2H, d), 8.72 (1H, s). 1-59 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.64-2.75 (2H, q), 7.40 (2H, s), 7.69 (1H, s), 7.83 (1H, d), 8.31 (1H, d), 8.84 (1H, s), 9.64 (1H, s). 1-60 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.39 (2H, d), 2.72 (2H, q), 2.90 (3H, s), 7.40 (2H, s), 7.45 (1H, s), 7.81 (2H, d), 8.13 (2H, d). 1-61 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.39 (3H, s), 2.75 (2H, q), 7.40 (2H, s), 7.68-7.54 (3H, m), 7.77 (2H, d), 7.88 (1H, d), 7.98 (1H, s), 8.23 (1H, d), 8.80 (1H, s). 1-62 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.38 (3H, s), 2.73 (2H, q), 7.42 (2H, s), 7.43-7.52 (2H, m), 7.61 (1H, dd), 7.92 (1H, d), 8.02 (1H, s), 8.09 (1H, d), 8.45 (1H, dd), 8.71 (1H, d). 1-63 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 7.41 (2H, s), 7.45-7.49 (2H, m), 7.63 (1H, s), 7.89-7.93 (2H, m), 8.41-8.28 (3H, m). 1-64 ¹H-NMR (CDCl₃) δ: 1.24 (6H, dz), 3.25-3.11 (1H, m), 7.38 (1H, s), 7.44 (1H, s), 7.57 (1H, s), 7.87 (2H, d), 8.09 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-66 ¹H-NMR (CDCl₃) δ: 1.25 (6H, d), 3.21-3.08 (1H, m), 7.40 (1H, s), 7.46 (1H, s), 7.68 (1H, s), 7.80 (1H, d), 8.17 (1H, s), 8.34 (1H, dd), 8.49 (1H, s), 8.55 (1H, d). 1-67 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 3.43 (3H, s), 4.52 (2H, s), 7.39 (1H, s), 7.53 (1H, s), 7.88 (2H, d), 8.11 (2H, d), 8.16 (1H, s), 8.68 (1H, s), 8.88 (1H, s). 1-68 ¹H-NMR (CDCl₃) δ: 2.39 (3H, s), 3.41 (3H, s), 4.51 (2H, s), 4.90 (2H, s), 7.26-7.39 (3H, m), 7.50-7.52 (2H, m), 8.20 (1H, s), 8.46 (1H, s), 8.77 (1H, s). 1-69 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 3.45 (3H, s), 4.55 (2H, s), 7.40 (1H, s), 7.55 (1H, s), 7.80 (1H, d), 8.17 (1H, s), 8.34 (1H, dd), 8.49 (1H, s), 8.57 (1H, d), 9.13 (1H, s). 1-70 ¹H-NMR (CDCl₃) δ: 2.38 (3H, s), 3.87 (3H, s), 6.99 (1H, s), 7.16 (1H, s), 7.69 (1H, s), 7.86 (2H, d), 8.10 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-72 ¹H-NMR (CDCl₃) δ: 2.37 (3H, s), 3.89 (3H, s), 7.01 (1H, s), 7.17 (1H, s), 7.77 (1H, d), 7.84 (1H, s), 8.16 (1H, s), 8.32 (1H, dd), 8.48 (1H, s), 8.53 (1H, d). 1-73 ¹H-NMR (CDCl₃) δ: 1.24 (6H, t, J = 7.6 Hz), 2.71 (4H, q, J = 7.6 Hz), 7.41 (2H, s), 7.46 (1H, s), 7.88 (2H, d), 8.08 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-74 ¹H-NMR (CDCl₃) δ: 1.24 (6H, t), 2.70 (4H, q), 7.41 (2H, s), 7.48 (1H, s), 7.81 (1H, d), 7.95 (1H, d), 8.16-8.18 (2H, m), 8.70 (1H, s). 1-75 ¹H-NMR (CDCl₃) δ: 1.25 (6H, t), 2.70 (4H, q), 7.42 (2H, s), 7.44 (1H, s), 7.72 (1H, d), 7.99 (1H, dd), 8.18 (1H, s), 8.33 (1H, d), 8.64 (1H, s). 1-77 ¹H-NMR (CDCl₃) δ: 1.25 (6H, t), 2.70 (4H, q), 7.43 (2H, s), 7.67 (1H, s), 7.80 (1H, d), 8.17 (1H, s), 8.33 (1H, dd), 8.49 (1H, s), 8.54 (1H, d). 1-78 ¹H-NMR (CDCl₃) δ: 7.79 (1H, s), 7.89 (2H, s), 7.89 (2H, d), 8.13 (2H, d), 8.16 (1H, s), 8.68 (1H, s). 1-79 ¹H-NMR (CDCl₃) δ: 7.92 (2H, d), 8.03 (1H, s), 8.14 (2H, d), 8.17 (2H, s), 8.69 (1H, s). 1-80 ¹H-NMR (CDCl₃) δ: 7.86 (2H, d), 8.15-8.10 (6H, m), 8.66 (1H, s). 1-81 ¹H-NMR (CDCl₃) δ: 7.82 (1H, d), 8.04-8.17 (4H, m), 8.38 (1H, d), 8.50 (1H, s), 8.60 (1H, s). 1-86 ¹H-NMR (acetone-d₆) δ: 1.15 (3H, t), 2.35 (3H, s), 2.75 (2H, q), 7.26 (2H, d), 7.84 (1H, s), 7.95 (1H, s), 8.14 (2H, d), 8.33 (2H, d), 9.42 (1H, s), 9.85 (1H, s). 1-87 ¹H-NMR (CDCl₃) δ: 2.39 (6H, s), 7.12 (2H, s), 7.73-7.77 (2H, m), 7.93 (1H, d), 8.01 (1H, d), 8.14 (1H, s), 8.15 (1H, s), 8.31 (1H, s), 8.65 (1H, s). 1-89 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.38 (2H, s), 7.45 (1H, s), 7.88 (2H, d), 8.09 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-96 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.46 (2H, s), 7.52 (1H, s), 7.72 (1H, d), 8.00 (1H, dd), 8.18 (1H, s), 8.33 (1H, d), 8.64 (1H, s). 1-99 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 7.46 (2H, s), 7.46 (1H, s), 7.87 (2H, d), 8.08 (2H, d), 8.16 (1H, s), 8.67 (1H, s). 1-101 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.28 (3H, s), 2.64 (2H, q), 7.45 (2H, s), 7.77 (1H, d), 7.96 (1H, s), 8.13 (1H, s), 8.32 (1H, dd), 8.47 (1H, s), 8.54 (1H, d). 1-102 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 1.26 (3H, t), 2.33 (3H, s), 2.46 (2H, q), 2.68 (2H, q), 7.44 (2H, s), 7.55 (1H, d), 7.76 (1H, s), 7.90 (1H, dd), 8.28 (1H, s), 8.56 (1H, s), 9.15 (1H, d), 9.98 (1H, s). 1-103 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.34 (3H, s), 2.70 (2H, q), 7.19 (1H, dd), 7.31 (1H, dd), 7.45 (2H, s), 7.52-7.58 (2H, m), 7.88 (1H, s), 7.95 (1H, d), 8.08 (1H, dd), 8.28 (1H, s), 8.54 (1H, s), 9.27 (1H, d), 10.60 (1H, d). 1-104 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.32 (3H, s), 2.68 (2H, q), 3.80 (3H, s), 7.44 (2H, s), 7.51 (1H, d), 7.73 (1H, s), 7.82 (1H, dd), 8.26 (1H, s), 8.54 (1H, s), 8.92 (1H, d), 9.30 (1H, s). 2-2 ¹H-NMR (CDCl₃) δ: 1.30 (3H, t), 2.49 (3H, s), 2.81 (2H, q), 7.44 (2H, s), 7.48 (1H, s), 7.59 (1H, d), 7.63-7.74 (2H, m), 7.80 (1H, dd), 7.89 (1H, d), 8.27 (1H, s), 8.46 (1H, s), 8.52 (1H, dd). 4-1 ¹H-NMR (acetone-d₆) δ: 2.34 (6H, s), 7.23 (2H, s), 7.56 (1H, s), 7.64 (1H, d), 8.23 (1H, s), 8.41 (1H, dd), 8.67 (1H, s), 9.03 (1H, d). 4-2 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 7.40 (2H, s), 7.45 (1H, s), 8.07 (1H, d), 8.15 (1H, s), 8.44 (1H, d), 9.01 (1H, s), 9.25 (1H, s). 5-1 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 3.98 (2H, s), 7.35 (2H, s), 7.45-7.48 (3H, m), 7.89 (2H, d). 5-2 ¹H-NMR (CDCl₃) δ: 2.04 (3H, s), 2.33 (6H, s), 4.51 (2H, d), 5.97 (1H, s), 7.35 (2H, s), 7.41 (2H, d), 7.53 (1H, s), 7.88 (2H, d). 5-3 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 2.27 (2H, q), 2.32 (6H, s), 4.51 (2H, d), 5.95 (1H, s), 7.35 (2H, s), 7.40 (2H, d), 7.59 (1H, s), 7.89 (2H, d). 5-4 ¹H-NMR (CDCl₃) δ: 1.21 (6H, d), 2.34 (6H, s), 2.42-2.44 (1H, m), 4.53 (2H, d), 5.85 (1H, s), 7.37-7.41 (5H, m), 7.89 (2H, d). 5-5 ¹H-NMR (CDCl₃) δ: 2.32 (6H, s), 4.11 (2H, s), 4.57 (2H, d), 7.04 (1H, s), 7.35 (2H, s), 7.42 (2H, d), 7.56 (1H, s), 7.90 (2H, d). 5-6 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 4.60 (2H, d), 5.96 (1H, t), 6.75 (1H, s), 7.36 (2H, s), 7.42-7.45 (3H, m), 7.91 (2H, d). 5-7 ¹H-NMR (CDCl₃) δ: 2.34 (6H, s), 3.14 (2H, q), 4.58 (2H, d), 6.21 (1H, s), 7.38-7.41 (5H, m), 7.89 (2H, d). 5-8 ¹H-NMR (CDCl₃) δ: 0.21-0.23 (2H, m), 0.60-0.66 (2H, m), 0.98-1.00 (1H, m), 2.23 (2H, d), 2.34 (6H, s), 4.56 (2H, d), 6.32 (1H, s), 7.35 (2H, s), 7.43-7.46 (3H, m), 7.90 (2H, d). 5-9 ¹H-NMR (CDCl₃) δ: 1.98-2.21 (6H, m), 2.34 (6H, s), 3.04-3.07 (1H, m), 4.51 (2H, d), 5.78 (1H, s), 7.35 (2H, s), 7.40 (2H, d), 7.52 (1H, s), 7.89 (2H, d). 5-10 ¹H-NMR (CDCl₃) δ: 1.59-1.91 (8H, m), 2.34 (6H, s), 2.57-2.59 (1H, m), 4.53 (2H, d), 5.86 (1H, s), 7.35 (2H, s), 7.41-7.43 (3H, m), 7.89 (2H, d,). 5-11 ¹H-NMR (CDCl₃) δ: 1.37-1.79 (10H, m), 2.14 (1H, m), 2.34 (6H, s), 4.52 (2H, d), 5.85 (1H, s), 7.35 (2H, s), 7.40 (2H, d), 7.44 (1H, s), 7.89 (2H, d). 5-12 ¹H-NMR (CDCl₃) δ: 1.88 (3H, dd), 2.34 (6H, s), 4.59 (2H, d), 5.82-5.87 (2H, m), 6.92 (1H, dd), 7.34-7.37 (3H, m), 7.44 (2H, d), 7.89 (2H, d). 5-13 ¹H-NMR (CDCl₃) δ: 1.77 (3H, dd), 1.87-1.87 (3H, m), 2.33 (6H, s), 4.58 (2H, d), 6.13 (1H, s), 6.49 (1H, dd), 7.35 (2H, s), 7.42 (2H, d), 7.51 (1H, s), 7.89 (2H, d). 5-14 ¹H-NMR (CDCl₃) δ: 2.34 (6H, s), 3.43 (3H, s), 3.96 (2H, s), 4.57 (2H, d, J = 6.0 Hz), 6.95 (1H, s), 7.35 (2H, s), 7.43-7.45 (3H, m), 7.90 (2H, d, J = 8.1 Hz). 5-15 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 2.53 (2H, tz), 3.38 (3H, s), 3.67 (2H, t), 4.53 (2H, d), 6.70 (1H, s), 7.35 (2H, s), 7.41 (2H, d), 7.49 (1H, s), 7.89 (2H, d). 5-16 ¹H-NMR (CDCl₃) δ: 1.21 (3H, d), 2.33 (6H, s), 2.43 (2H, d), 3.34 (3H, s), 3.72-3.75 (1H, m), 4.53 (2H, t), 6.74 (1H, s), 7.35 (2H, s), 7.41 (2H, d), 7.54 (1H, s), 7.89 (2H, d). 5-17 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 4.52 (2H, d), 4.93 (2H, s), 6.97 (1H, s), 7.34-7.36 (4H, m), 7.57 (1H, s), 7.87 (2H, d), 8.00 (1H, s), 8.03 (1H, s). 5-18 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 3.61 (2H, s), 4.49 (2H, d), 5.82 (1H, s), 7.05 (2H, dd), 7.24-7.27 (4H, m), 7.31-7.35 (4H, m), 7.41 (1H, s), 7.86 (2H, d,). 5-19 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 4.76 (2H, d), 7.35 (2H, s), 7.37-7.42 (1H, m), 7.49-7.52 (3H, m), 7.92 (2H, d), 8.35-8.36 (1H, m), 8.57-8.64 (1H, m). 5-21 ¹H-NMR (CDCl₃) δ: 2.06 (3H, s), 2.35 (6H, s), 4.50 (2H, dz), 5.99 (1H, s), 7.16 (1H, d), 7.22 (1H, dd), 7.36 (2H, s), 7.96 (1H, d), 8.11 (1H, t). 5-22 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.27-2.33 (8H, m), 4.51 (2H, d), 5.99 (1H, s), 7.15 (1H, d), 7.21 (1H, dd), 7.36 (2H, s), 7.97 (1H, d), 8.10 (1H, t). 5-24 ¹H-NMR (CDCl₃) δ: 0.23-0.26 (2H, m), 0.64-0.67 (2H, m), 1.00-1.03 (1H, m), 2.26 (2H, d), 2.35 (6H, s), 4.56 (2H, d), 6.36 (1H, s), 7.17 (1H, d), 7.24 (1H, d), 7.36 (2H, s), 7.96 (1H, d), 8.13 (1H, t). 5-25 ¹H-NMR (CDCl₃) δ: 2.35 (6H, s), 3.14 (2H, q), 4.55 (2H, d), 6.41 (1H, s), 7.13 (1H, d), 7.20 (1H, d), 7.36 (2H, s), 7.96 (1H, d), 8.09 (1H, t). 5-27 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 3.98 (2H, s), 7.37 (2H, s), 7.47 (1H, s), 7.44 (2H, d), 7.90 (2H, d). 5-28 ¹H-NMR (acetone-d₆) δ: 1.17 (3H, t), 1.94 (3H, s), 2.35 (3H, s), 2.75 (2H, q), 4.45 (2H, d), 7.46-7.44 (4H, m), 7.61 (1H, s), 7.99 (2H), 9.17 (1H, s). 5-29 ¹H-NMR (CDCl₃) δ: 1.19-1.22 (6H, m), 2.28 (2H, q), 2.33 (3H, s), 2.68 (2H, q), 4.53 (2H, d), 5.88 (1H, s), 7.37 (2H, s), 7.42-7.45 (3H, m), 7.89 (2H, d). 5-30 ¹H-NMR (CDCl₃) δ: 0.75-1.08 (4H, m), 1.21 (3H, t), 1.36-1.44 (1H, m), 2.33 (3H, s), 2.68 (2H, q), 4.53 (2H, d), 6.10 (1H, s), 7.36 (2H, s), 7.42 (2H, d), 7.52 (1H, s), 7.88 (2H, d). 5-31 ¹H-NMR (CDCl₃) δ: 0.19-0.24 (2H, m), 0.61-0.64 (2H, m), 0.97-0.99 (1H, m), 1.21 (3H, t), 2.21 (2H, d), 2.33 (3H, s), 2.68 (2H, q), 4.55 (2H, d), 6.37 (1H, s), 7.36 (2H, s), 7.42 (2H, d), 7.59 (1H, s), 7.90 (2H, d). 5-32 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 3.14 (2H, q), 4.57 (2H, d), 6.27 (1H, s), 7.38-7.41 (5H, m), 7.88 (2H, d). 5-33 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.69 (2H, q), 3.27 (2H, s), 4.57 (2H, d), 7.37 (2H, s), 7.44-7.46 (3H, m), 7.90 (2H, d). 5-34 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.76 (2H, d), 7.14 (1H, dd), 7.29 (1H, d), 7.36 (2H, s), 7.46-7.54 (4H, m), 7.91 (2H, d), 8.12 (1H, td). 5-35 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t,), 2.33 (3H, s), 2.67 (2H, q), 4.71 (2H, d), 6.63 (1H, s), 7.19-7.25 (1H, m), 7.41-7.51 (7H, m), 7.90 (2H, d). 5-36 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 2.29 (3H, s), 2.66 (2H, q), 4.91 (2H, s), 6.99 (2H, t), 7.34 (2H, s), 7.49-7.54 (4H, m), 7.93 (3H, d). 5-37 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.75 (2H, d), 6.70 (1H, s), 7.30-7.44 (4H, m), 7.53 (2H, d), 7.68-7.71 (1H, m), 7.92 (2H, d). 5-38 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.71 (2H, d), 6.61 (1H, s), 7.36 (2H, s), 7.40 (1H, d), 7.47-7.52 (4H, m), 7.66-7.69 (1H, m), 7.79-7.80 (1H, m), 7.90 (2H, d). 5-39 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.71 (2H, d), 6.56 (1H, s), 7.37 (2H, s), 7.43-7.48 (5H, m), 7.74 (2H, d), 7.90 (2H, d). 5-40 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 4.77 (2H, d), 7.37-7.42 (4H, m), 7.51 (2H, d), 7.92 (2H, d), 8.35-8.37 (1H, m), 8.58-8.65 (1H, m). 5-41 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.75 (2H, d), 7.05 (1H, s), 7.34-7.38 (3H, m), 7.54-7.51 (3H, m), 7.92 (2H, d), 8.14 (1H, dd), 8.48 (1H, dd). 5-42 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 4.81-4.83 (4H, m), 7.37 (2H, s), 7.40 (1H, s), 7.46 (2H, d), 7.88 (2H, d). 5-44 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.34 (3H, s), 2.70 (2H, q), 4.51 (2H, d), 5.96 (1H, s), 7.16 (1H, d), 7.22 (1H, d), 7.37 (2H, s), 7.97 (1H, d), 8.12 (1H, t). 5-45 ¹H-NMR (CDCl₃) δ: 1.19-1.26 (6H, m), 2.29 (2H, q), 2.34 (3H, s), 2.70 (2H, q), 4.52 (2H, d), 5.92 (1H, s), 7.16 (1H, d), 7.23 (1H, dd), 7.37 (2H, s), 7.97 (1H, d), 8.13 (1H, t). 5-46 ¹H-NMR (CDCl₃) δ: 0.23-0.26 (2H, m), 0.64-0.67 (2H, m), 1.00-1.03 (1H, m), 1.22 (3H, t), 2.26 (2H, d), 2.35 (3H, s), 2.70 (2H, q), 4.56 (2H, d), 6.36 (1H, s), 7.17 (1H, d), 7.24 (1H, d), 7.37 (2H, s), 7.97 (1H, d), 8.14 (1H, t). 5-47 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.70 (2H, q), 3.15 (2H, q), 4.56 (2H, d), 6.31 (1H, s), 7.14 (1H, d), 7.21 (1H, d), 7.37 (3H, s), 7.96 (1H, d), 8.11 (1H, t). 5-48 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.35 (3H, d), 2.70 (2H, q), 4.76 (2H), 7.22 (1H, d), 7.32 (1H, d), 7.38 (2H, d), 7.41-7.42 (1H, m), 7.97 (1H, d), 8.17 (1H, t), 8.37 (1H, td), 8.59-8.66 (1H, m). 5-49 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 1.48 (9H, s), 2.35 (3H, s), 2.70 (2H, q), 4.39 (2H, d), 5.02 (1H, s), 7.14-7.25 (2H, m), 7.37 (2H, s), 7.97 (1H, d), 8.14 (1H, dd). 5-51 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.04 (3H, s), 2.34 (3H, s), 2.69 (2H, q), 4.56 (2H, d), 6.04 (1H, s), 7.27-7.29 (1H, m), 7.38 (2H, s), 7.81-7.88 (2H, m). 5-52 ¹H-NMR (CDCl₃) δ: 1.13-1.26 (6H, m), 2.28 (2H, q), 2.34 (3H, s), 2.70 (2H, q), 4.57 (2H, d), 5.94 (1H, s), 7.28-7.30 (1H, m), 7.38 (2H, s), 7.83-7.86 (2H, m). 5-53 ¹H-NMR (CDCl₃) δ: 0.77-0.81 (2H, m), 0.98-1.05 (2H, m), 1.22 (3H, t), 1.38-1.43 (1H, m), 2.34 (3H, s), 2.70 (2H, q), 4.58 (2H, d), 6.18 (1H, t), 7.28-7.30 (1H, m), 7.37 (2H, s), 7.83-7.86 (2H, m). 5-54 ¹H-NMR (CDCl₃) δ: 0.22-0.24 (2H, m), 0.64-0.67 (2H, m), 0.98-1.00 (1H, m), 1.23 (3H, t), 2.23 (2H, d), 2.35 (3H, s), 2.70 (2H, q), 4.61 (2H, d), 6.39 (1H, s), 7.30 (1H, d), 7.38 (2H, s), 7.83-7.88 (2H, m). 5-55 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 3.14 (2H, q), 4.63 (2H, d), 6.25 (1H, s), 7.28-7.31 (1H, m), 7.38 (2H, s), 7.79-7.90 (2H, m). 5-57 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 3.99 (2H, s), 7.32 (1H, dd), 7.38 (2H, s), 7.83 (1H, dd), 8.03 (1H, dz). 5-58 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.05 (3H, s), 2.32 (3H, s), 2.68 (2H, q), 4.50 (2H, d), 6.05 (1H, t), 7.24-7.30 (1H, m), 7.37 (2H, s), 7.84 (1H, dd), 8.01 (1H, d). 5-59 ¹H-NMR (CDCl₃) δ: 1.16-1.24 (6H, m), 2.28 (2H, q), 2.33 (3H, s), 2.68 (2H, q), 4.51 (2H, d), 6.02 (1H, t), 7.24-7.29 (1H, m), 7.37 (2H, s), 7.84 (1H, dd), 8.01 (1H, d). 5-61 ¹H-NMR (CDCl₃) δ: 0.22-0.24 (2H, m), 0.63-0.69 (2H, m), 0.96-1.02 (1H, m), 1.21 (3H, t), 2.23 (2H, d), 2.33 (3H, s), 2.68 (2H, q), 4.55 (2H, d), 6.45 (1H, t), 7.27 (1H, dd), 7.37 (2H, s), 7.85 (1H, dd), 8.00 (1H, d). 5-62 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 3.11 (2H, q), 4.55 (2H), 6.49 (1H, s), 7.23 (1H, dd), 7.38 (2H, s), 7.82 (1H, dd), 8.01 (1H, d). 5-63 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 1.47 (9H, s), 2.34 (3H, s), 2.69 (2H, q), 4.40 (2H, d), 5.06 (1H, s), 7.22-7.24 (1H, m), 7.37 (2H, s), 7.84 (1H, dd), 8.01 (1H, d). 5-64 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.40 (3H, s), 2.74 (2H, q), 3.95 (2H, s), 7.37-7.34 (3H, m), 7.49 (1H, s), 7.68 (1H, s), 7.83 (1H, d). 5-65 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.04 (3H, s), 2.38 (3H, s), 2.73 (2H, q), 4.44 (2H, d), 6.21 (1H, s), 7.24-7.28 (1H, m), 7.35-7.38 (3H, m), 7.72-7.74 (2H, m). 5-66 ¹H-NMR (CDCl₃) δ: 1.18-1.23 (6H, m), 2.28 (2H, q), 2.39 (3H, s), 2.73 (2H, q), 4.46 (2H, dz), 6.05 (1H, s), 7.29-7.29 (1H, m), 7.35-7.39 (3H, m), 7.66 (1H, s), 7.76 (1H, d). 5-67 ¹H-NMR (CDCl₃) δ: 0.20-0.24 (2H, m), 0.56-0.68 (2H, m), 0.96-1.03 (1H, m), 1.23 (3H, t), 2.24 (2H, d), 2.40 (3H, s), 2.74 (2H, q), 4.51 (2H, d), 6.37 (1H, s), 7.31 (1H, dd), 7.38 (2H, s), 7.41 (1H, s), 7.62 (1H, s), 7.81 (1H, d). 5-68 ¹H-NMR (CDCl₃) δ: 1.21-1.24 (6H, m), 2.37 (3H, s), 2.72 (2H, q), 3.12 (2H, q), 4.49 (2H, d), 6.68 (1H, s), 7.23 (1H, d), 7.32 (1H, s), 7.37 (2H, s), 7.64 (1H, s), 7.70 (1H, d). 5-69 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 1.47 (9H, s), 2.40 (3H, s), 2.74 (2H, q), 4.35 (2H, d), 5.01 (1H, s), 7.32 (1H, d), 7.38 (2H, s), 7.41 (1H, s), 7.61 (1H, s), 7.82 (1H, d). 5-72 ¹H-NMR (CDCl₃) δ: 1.12-1.25 (6H, m), 2.24 (2H, q), 2.32 (3H, s), 2.67 (2H, q), 4.53 (2H, d), 6.01 (1H, s), 7.36 (2H, s), 7.48 (1H, t), 7.64-7.66 (3H, m). 5-76 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.56 (2H, s), 7.37 (2H, s), 7.44 (1H, s), 7.67 (1H, d), 7.77 (1H, d), 7.93 (1H, s). 5-77 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.56 (2H, d), 6.10 (1H, s), 7.36 (2H, s), 7.52 (1H, d), 7.60 (1H, s), 7.75 (1H, dd), 7.96 (1H, d). 5-78 ¹H-NMR (CDCl₃) δ: 1.11-1.28 (6H, m), 2.24 (2H, q), 2.31 (3H, s), 2.67 (2H, q), 4.56 (2H, d), 6.10 (1H, t), 7.36 (2H, s), 7.49 (1H, d), 7.69 (1H, s), 7.75 (1H, dd), 7.96 (1H, d). 5-79 ¹H-NMR (CDCl₃) δ: 0.75-0.78 (2H, m), 0.92-0.97 (2H, m), 1.21 (3H, t), 1.38-1.44 (1H, m), 2.32 (3H, s), 2.67 (2H, q), 4.59 (2H, d), 6.24 (1H, s), 7.37 (2H, s), 7.51 (1H, d), 7.56 (1H, s), 7.74 (1H, d), 7.95 (1H, s). 5-80 ¹H-NMR (CDCl₃) δ: 0.19-0.23 (2H, m), 0.61-0.67 (2H, m), 0.95-0.98 (1H, m), 1.21 (3H, t), 2.19 (2H, d), 2.33 (3H, s), 2.67 (2H, q), 4.61 (2H, d), 6.54 (1H, s), 7.37 (2H, s), 7.53-7.55 (2H, m), 7.76 (1H, t), 7.97 (1H, d). 5-81 ¹H-NMR (CDCl₃) δ: 1.17-1.25 (6H, m), 2.30 (3H, s), 2.65 (2H, qz), 3.10 (2H, q), 4.59 (2H, d), 6.57 (1H, d), 7.36 (2H, s), 7.44 (1H, d), 7.58 (1H, s), 7.70 (1H, d), 7.91 (1H, s). 5-82 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.82 (2H, d), 7.35-7.44 (4H, m), 7.62 (1H, d), 7.78 (1H, d), 7.98 (1H, d), 8.35-8.36 (1H, m), 8.58 (1H, dt). 5-83 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.00 (2H, s), 7.37 (2H, s), 7.42 (1H, s), 7.57 (1H, d), 7.83 (1H, dd), 8.10 (1H, d). 5-84 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.32 (3H, s), 2.66 (2H, q), 4.61 (2H, d), 6.23 (1H, s), 7.37 (2H, s), 7.52-7.54 (2H, m), 7.81 (1H, dd), 8.14 (1H, d), 8.29 (1H, s). 5-85 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.31 (3H, s), 2.66 (2H, q), 4.54 (2H, d), 6.14 (1H, t), 7.36 (2H, s), 7.51 (1H, d), 7.65 (1H, s), 7.80 (1H, dd), 8.14 (1H, d). 5-86 ¹H-NMR (CDCl₃) δ: 1.14-1.24 (6H, m), 2.26 (2H, q), 2.32 (3H, s), 2.67 (2H, q), 4.56 (2H, d), 6.06 (1H, s), 7.37 (2H, s), 7.51-7.53 (2H, m), 7.80 (1H, dd), 8.14 (1H, d). 5-88 ¹H-NMR (CDCl₃) δ: 0.20-0.24 (2H, m), 0.61-0.67 (3H, m), 0.96-0.98 (1H, m), 1.22 (3H, t), 2.19 (2H, d), 2.33 (3H, s), 2.67 (2H, q), 4.59 (2H, d), 6.58 (1H, s), 7.37 (2H, s), 7.47 (1H, s), 7.54 (1H, d), 7.80 (1H, d), 8.14 (1H, s). 5-89 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 3.13 (2H, q), 4.61 (2H, d), 6.38 (1H, s), 7.37 (3H, s), 7.51 (1H, d), 7.79 (1H, d), 8.13 (1H, s). 5-90 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 1.87 (3H, dd,), 2.33 (3H, s), 2.67 (2H, q), 4.63 (2H, d), 5.85 (1H, d), 6.00 (1H, s), 6.89 (1H, dd), 7.35-7.38 (3H, m), 7.56 (1H, d), 7.78 (1H, d), 8.13 (1H, s). 5-91 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 3.43 (3H, s), 3.93 (2H, s), 4.62 (2H, d), 7.11 (1H, s), 7.37 (2H, s), 7.51-7.53 (2H, m), 7.82 (1H, dd), 8.15 (1H, d). 5-92 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, d), 2.67 (2H, q), 4.75 (2H, d), 6.74 (1H, s), 7.12 (2H, t), 7.37 (2H, s), 7.43 (1H, s), 7.61 (1H, d), 7.79-7.82 (3H, m), 8.16 (1H, d). 5-93 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.80 (2H), 7.36-7.39 (3H, m), 7.43 (1H, s), 7.50 (1H, t), 7.61 (1H, d), 7.83 (1H, dd), 8.16 (1H, d), 8.36 (1H, td), 8.57 (1H, ddd). 5-94 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 2.26 (3H, s), 2.62 (2H, q), 4.74 (2H, d), 7.28 (1H, dd), 7.34 (2H, s), 7.38 (1H, dd), 7.56 (1H, d), 7.82 (1H, dd), 7.94 (1H, s), 8.00 (1H, dd), 8.14 (1H, d), 8.42 (1H, dd). 5-95 ¹H-NMR (acetone-d₆) δ: 1.07 (3H, t), 1.18 (3H, t), 2.76 (2H, q), 2.79 (3H, s), 3.22-3.13 (2H, m), 4.44 (2H, d), 5.66 (1H, s), 6.03 (1H, s), 7.46 (2H, s), 7.57 (1H, d), 8.00 (1H, dd), 8.19 (1H, d), 9.28 (1H, s). 5-96 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 2.28 (3H, s), 2.65 (2H, q), 2.93 (3H, s), 4.46 (2H, d), 5.14 (1H, t), 7.36 (2H, s), 7.61 (1H, d), 7.66 (1H, s), 7.84 (1H, dd), 8.14 (1H, d). 5-97 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.68 (2H, q), 2.82 (6H, s), 4.41 (2H, d), 4.67 (1H, t), 7.33 (1H, s), 7.38 (2H, s), 7.64 (1H, d), 7.84 (1H, dd), 8.15 (1H, d). 5-98 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.41 (3H, s), 2.69 (2H, q), 3.94 (2H, s), 7.36 (2H, s), 7.44-7.50 (2H, m), 7.74-7.72 (2H, m). 5-99 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.04 (3H, s), 2.33 (3H, s), 2.41 (3H, s), 2.68 (2H, q), 4.49 (2H, d), 5.80 (1H, s), 7.34-7.36 (3H, m), 7.47 (1H, s), 7.69-7.72 (2H, m). 5-100 ¹H-NMR (CDCl₃) δ: 1.16-1.26 (6H, m), 2.27 (2H, q), 2.34 (3H, s), 2.42 (3H, s), 2.69 (2H, q), 4.51 (2H, d), 5.69 (1H, s), 7.36-7.39 (4H, m), 7.70 (1H, d), 7.75 (1H, s). 5-101 ¹H-NMR (CDCl₃) δ: 0.21-0.25 (2H, m), 0.61-0.67 (2H, m), 0.98-1.01 (1H, m), 1.22 (3H, t), 2.24 (2H, d), 2.34 (3H, s), 2.43 (3H, s), 2.69 (2H, q), 4.55 (2H, d), 6.15 (1H, s), 7.37-7.39 (4H, m), 7.71 (1H, d), 7.75 (1H, s). 5-102 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.41 (3H, s), 2.68 (2H, q), 3.13 (2H, q), 4.55 (2H, d), 6.11 (1H, s), 7.34-7.36 (4H, m), 7.68 (1H, d), 7.74 (1H, s). 5-103 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.48 (3H, s), 2.69 (2H, q), 4.75 (2H, d), 7.15 (1H, s), 7.37-7.42 (4H, m), 7.46 (1H, d), 7.73 (1H, d), 7.79 (1H, s), 8.35-8.36 (1H, m), 8.62 (1H, ddd). 5-104 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 1.47 (9H, s), 2.33 (3H, s), 2.40 (3H, s), 2.68 (2H, q), 4.37 (2H, d), 4.85 (1H, s), 7.36-7.44 (4H, m), 7.70-7.73 (2H, m). 5-106 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.05 (3H, s), 2.34 (3H, s), 2.68 (2H, q), 4.69 (2H, d), 5.92 (1H, s), 7.38 (2H, s), 7.46 (1H, s), 7.77 (1H, d), 8.05 (1H, d), 8.23 (1H, s). 5-107 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 1.21 (3H, t), 2.26 (2H, q), 2.33 (3H, s), 2.68 (2H, q), 4.68 (2H, d), 5.94 (1H, s), 7.38 (2H, s), 7.61 (1H, s), 7.73 (1H, d), 8.05 (1H, d), 8.23 (1H, s). 5-108 ¹H-NMR (CDCl₃) δ: 0.77-0.81 (2H, m), 0.97-1.02 (2H, m), 1.22 (3H, t), 1.37-1.43 (1H, m), 2.34 (3H, s), 2.68 (2H, q), 4.70 (2H, d), 6.11 (1H, s), 7.38 (2H, s), 7.53 (1H, s), 7.74 (1H, d), 8.05 (1H, d), 8.22 (1H, s). 5-109 ¹H-NMR (CDCl₃) δ: 0.19-0.21 (2H, m), 0.60-0.66 (2H, m), 0.92-0.95 (1H, m), 1.22 (3H, t), 2.20 (2H, d), 2.34 (3H, s), 2.68 (2H, q), 4.72 (2H, d), 6.43 (1H, s), 7.38 (2H, s), 7.55 (1H, s), 7.76 (1H, d), 8.05 (1H, d), 8.24 (1H, s). 5-110 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.67 (2H, q), 3.14 (2H, q), 4.75 (2H, d), 6.21 (1H, s), 7.37-7.40 (3H, m), 7.41 (1H, s), 7.73 (1H, d), 8.06 (1H, d), 8.24 (1H, s). 5-111 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.67 (2H, q), 4.89 (2H, d), 6.56 (1H, s), 7.13 (2H, t), 7.38 (2H, s), 7.45 (1H, s), 7.77-7.85 (3H, m), 8.05 (1H, d), 8.26 (1H, s). 5-112 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.94 (2H, d), 7.38-7.41 (3H, m), 7.49 (1H, s), 7.81 (1H, d), 8.07 (1H, d), 8.26 (1H, s), 8.35-8.37 (1H, m), 8.59 (1H, ddd). 5-113 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.32 (3H, s), 2.66 (2H, q), 5.37 (2H, s), 7.37 (2H, s), 7.45 (1H, d), 7.60 (1H, s), 7.82-7.79 (2H, m), 7.93-7.91 (2H, m), 8.12 (1H, dd), 8.64 (1H, d). 5-114 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 1.95 (3H, s), 2.31 (3H, s), 2.67 (2H, q), 4.72 (2H, d), 6.44 (1H, t), 7.38 (2H, s), 7.81 (1H, d), 8.04 (1H, s), 8.18 (1H, dd), 8.64 (1H, d). 5-115 ¹H-NMR (CDCl₃) δ: 1.09 (3H, t), 1.21 (3H, t), 2.20 (2H, q), 2.32 (3H, s), 2.67 (2H, q), 4.73 (2H, d), 6.41 (1H, t), 7.38 (2H, s), 7.80 (1H, d), 8.00 (1H, s), 8.17 (1H, dd), 8.64 (1H, d). 5-116 ¹H-NMR (CDCl₃) δ: 0.69-0.74 (2H, m), 0.78-0.83 (2H, m), 1.18 (3H, t), 1.36-1.44 (1H, m), 2.29 (3H, s), 2.65 (2H, q), 4.72 (2H, d), 6.72 (1H, t), 7.36 (2H, s), 7.68 (1H, d), 8.16 (1H, dd), 8.38 (1H, s), 8.64 (1H, d). 5-117 ¹H-NMR (CDCl₃) δ: 0.10-0.15 (2H, m), 0.56-0.62 (2H, m), 0.82-0.90 (1H, m), 1.20 (3H, t), 2.07 (2H, d), 2.32 (3H, s), 2.67 (2H, q), 4.76 (2H, d), 6.91 (1H, t), 7.38 (2H, s), 7.79 (1H, d), 8.23-8.19 (2H, m), 8.66 (1H, d). 5-118 ¹H-NMR (acetone-d₆) δ: 1.06 (3H, t), 2.25 (3H, s), 2.66 (2H, q), 3.27 (2H, q), 4.71 (2H, d), 7.36 (2H, s), 7.72 (1H, d), 8.02 (1H, br s), 8.23 (1H, dd), 8.54 (1H, d), 9.44 (1H, s). 5-127 ¹H-NMR (CDCl₃) δ: 1.19 (3H, q), 2.27 (2H, q), 2.33 (3H, s), 4.53 (2H, d), 5.87 (1H, s), 7.34 (2H, s), 7.41-7.43 (3H, m), 7.89 (2H, d). 5-139 ¹H-NMR (CDCl₃) δ: 1.19-1.21 (6H, m), 2.25-2.33 (5H, m), 2.67 (2H, q, J = 25.8 Hz), 4.53 (2H, d, J = 5.9 Hz), 5.88 (1H, s), 7.35 (2H, s), 7.42-7.45 (3H, m), 7.89 (2H, d, J = 8.1 Hz). 5-142 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t, J = 7.6 Hz), 2.31 (3H, s), 2.67 (2H, q, J = 7.5 Hz), 3.11 (2H, q, J = 10.6 Hz), 4.55 (2H, d, J = 5.9 Hz), 6.52 (1H, s), 7.35-7.38 (4H, m), 7.53 (1H, s), 7.84 (2H, d, J = 8.1 Hz). 5-144 ¹H-NMR (CDCl₃) δ: 1.11 (3H, t, J = 7.6 Hz), 1.81 (3H, s), 2.21 (3H, s), 2.60 (2H, q, J = 7.5 Hz), 4.40 (2H, d, J = 6.0 Hz), 6.79 (1H, t, J = 6.0 Hz), 7.28-7.29 (3H, m), 7.56-7.60 (2H, m), 8.72 (1H, s). 5-145 ¹H-NMR (CDCl₃) δ: 1.17-1.21 (6H, m), 2.26 (2H, q, J = 7.6 Hz), 2.33 (3H, s), 2.67 (2H, q, J = 7.4 Hz), 4.55 (2H, d, J = 6.2 Hz), 5.92 (1H, s), 7.36 (2H, s), 7.43 (1H, s), 7.51 (1H, t, J = 7.6 Hz), 7.63-7.65 (2H, m). 5-146 ¹H-NMR (CDCl₃) δ: 0.74-0.78 (2H, m), 0.92-0.96 (2H, m), 1.21 (3H, t, J = 12.6 Hz), 1.37-1.39 (1H, m), 2.32 (3H, s), 2.67 (2H, q, J = 7.5 Hz), 4.55 (2H, d, J = 6.0 Hz), 6.16 (1H, d, J = 6.2 Hz), 7.35 (2H, s), 7.48 (1H, t, J = 7.7 Hz), 7.61-7.65 (3H, m). 5-147 ¹H-NMR (CDCl₃) δ: 0.19-0.21 (2H, m), 0.59-0.63 (2H, m), 0.92-0.97 (1H, m), 1.20 (3H, t, J = 7.6 Hz), 2.17 (2H, d, J = 3.6 Hz), 2.32 (3H, s), 2.67 (2H, q, J = 7.5 Hz), 4.57 (2H, d, J = 6.0 Hz), 6.45 (1H, s), 7.35 (2H, s), 7.49 (1H, t, J = 7.7 Hz), 7.65-7.67 (3H, m). 5-148 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t, J = 8.0 Hz), 2.33 (3H, s), 2.67 (2H, q, J = 7.3 Hz), 3.12 (2H, q, J = 10.6 Hz), 4.60 (2H, d, J = 5.9 Hz), 6.32 (1H, s), 7.36 (2H, s), 7.42 (1H, s), 7.49 (1H, t, J = 7.7 Hz), 7.63-7.65 (2H, m). 5-149 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.02 (2H, s), 7.35 (2H, s), 7.48 (1H, s), 7.57 (1H, d), 7.79 (1H, dd), 7.93 (1H, s). 5-150 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.01 (2H, s), 2.32 (3H, s), 2.66 (2H, q), 4.56 (2H, d), 6.13 (1H, s), 7.35 (2H, s), 7.52 (1H, d), 7.66 (1H, s), 7.76 (1H, dd), 7.96 (1H, d). 5-151 ¹H-NMR (CDCl₃) δ: 1.14-1.25 (6H, m), 2.26 (2H, q), 2.32 (3H, s), 2.67 (2H, q), 4.58 (2H, d), 6.04 (1H, s), 7.35 (2H, s), 7.52-7.54 (2H, m), 7.76 (1H, dd), 7.96 (1H, d). 5-152 ¹H-NMR (CDCl₃) δ: 0.76-0.80 (2H, m), 0.97-1.02 (2H, m), 1.21 (3H), 1.38-1.44 (1H, m), 2.33 (3H, s), 2.67 (2H, q), 4.61 (2H, d), 6.18 (1H, s), 7.36 (2H, s), 7.40 (1H, s), 7.55 (1H, d), 7.75 (1H, d), 7.95 (1H, s). 5-153 ¹H-NMR (CDCl₃) δ: 0.19-0.22 (2H, m), 0.61-0.64 (2H, m), 0.93-0.98 (1H, m), 1.20 (3H, t), 2.18 (2H, d), 2.32 (3H, s), 2.67 (2H, q), 4.61 (2H, d), 6.56 (1H, s), 7.35 (2H, s), 7.53 (1H, d), 7.61 (1H, s), 7.77 (1H, dd), 7.97 (1H, d). 5-154 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 3.14 (2H, q), 4.64 (2H, d), 6.31 (1H, s), 7.36 (2H, s), 7.54 (1H, d), 7.76 (1H, d), 7.97 (1H, s). 5-155 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.32 (3H, s), 2.66 (2H, q), 4.82 (2H, d), 7.35-7.40 (3H, m), 7.47 (1H, s), 7.61 (1H, d), 7.78 (1H, dd), 7.98 (1H, d), 8.35-8.36 (1H, m), 8.57 (1H, ddd). 5-157 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.01 (3H, s), 2.32 (3H, s), 2.67 (2H, q), 4.55 (2H, d), 6.14 (1H, t), 7.35 (2H, s), 7.51 (1H, d), 7.65 (1H, s), 7.80 (1H, dd), 8.14 (1H). 5-158 ¹H-NMR (CDCl₃) δ: 1.16-1.21 (6H, m), 2.27 (2H, q), 2.32 (3H, s), 2.67 (2H, q), 4.56 (2H, d), 6.05 (1H, t), 7.35 (2H, s), 7.50-7.52 (2H, m), 7.79 (1H, d), 8.13 (1H, s). 5-159 ¹H-NMR (CDCl₃) δ: 0.77-0.80 (2H, m), 0.96-1.00 (2H, m), 1.21 (3H, t), 2.33 (3H, s), 2.68 (2H, q), 4.59 (2H, d), 6.21 (1H, s), 7.36 (2H, s), 7.40 (1H, s), 7.54 (1H, d), 7.80 (1H, d), 8.13 (1H, s). 5-160 ¹H-NMR (acetone-d₆) δ: −0.02-0.01 (2H, m), 0.29-0.32 (3H, m), 0.94 (3H, t), 1.97 (2H, d), 2.59 (3H, s), 4.30 (2H, d), 7.24 (2H, s), 7.34 (1H, d), 7.80 (1H, dd), 8.00 (1H, d). 5-161 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.66 (2H, q), 3.24 (2H, q), 4.62 (2H, d), 6.34 (1H, s), 7.36 (2H, s), 7.53 (1H, d), 7.81 (1H, d), 8.14 (1H, s). 5-174 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.79 (2H, d), 7.35-7.42 (4H, m), 7.58-7.69 (3H, m), 8.35-8.36 (1H, m), 8.55-8.62 (1H, m). 5-175 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 4.80 (2H, d), 7.36-7.37 (3H, m), 7.43 (1H, s), 7.67 (1H, d), 7.84 (1H, d), 8.15-8.18 (2H, m), 8.49 (1H, dd). 5-177 ¹H-NMR (acetone-d₆) δ: 1.17 (3H, t), 2.69-2.80 (8H, m), 3.60 (1H, d), 3.79 (1H, d), 4.58 (2H, d), 7.46 (2H, s), 7.73 (1H, d), 7.99-8.03 (2H, m), 8.22 (1H, d), 9.32 (1H, s). 5-178 ¹H-NMR (acetone-d₆) δ: 1.17 (3H, t), 2.73-2.79 (5H, m), 3.13 (3H, s), 4.16 (2H, s), 4.59 (2H, dz), 7.46 (2H, s), 7.69 (1H, d), 8.01 (1H, dd), 8.23 (1H, d), 9.32 (1H, s). 5-179 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.17 (2H, t), 2.34 (3H, d), 2.67 (2H, q), 3.23 (3H, s), 4.61 (2H, d), 7.36 (2H, s), 7.50-7.53 (2H, m), 7.81 (1H, dd), 8.15 (1H, d). 5-181 ¹H-NMR (acetone-d₆) δ: 1.18 (3H, t), 2.36 (3H, s), 2.76 (2H, q), 3.14 (3H, d), 4.17 (2H, s), 4.61 (2H, d), 7.46 (2H, s), 7.69 (1H, d), 8.01-8.04 (2H, m), 8.25-8.25 (2H, m). 5-182 ¹H-NMR (CDCl₃) δ: 2.35 (6H, s), 4.75 (2H, d), 7.12 (1H, s), 7.25-7.41 (5H, m), 7.98 (1H, d), 8.16-8.19 (2H, m), 8.50 (1H, dd). 5-183 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 4.75 (2H, d), 7.15 (1H, t), 7.37-7.41 (3H, m), 7.89 (1H, dd), 8.01 (1H, d), 8.17 (1H, dt), 8.50 (1H, dt). 5-184 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.31 (3H, s), 2.48 (3H, s), 2.67 (2H, q), 3.84 (2H, s), 7.36 (2H, s), 7.45 (2H, d), 7.57 (1H, s), 7.87 (2H, d). 5-185 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 2.98 (3H, s), 4.62-4.65 (2H, m), 7.32-7.38 (4H, m), 7.66-7.69 (1H, m), 7.90-7.96 (2H, m). 5-186 ¹H-NMR (CDCl₃) δ: 1.13-1.21 (6H, m), 2.35 (3H, s), 2.42 (2H, q), 2.69 (2H, q), 2.98 (3H, d), 4.65 (2H, d), 7.31-7.38 (4H, m), 7.57 (1H, br s), 7.89-7.92 (2H, m). 5-187 ¹H-NMR (CDCl₃) δ: 0.14-0.19 (2H, m), 0.55-0.58 (2H, m), 1.07-1.10 (1H, m), 1.22 (3H, t), 2.34 (3H, br s), 2.70 (2H, q), 2.97 (3H, d), 4.64 (2H, d), 7.31-7.39 (4H, m), 7.67 (1H, d), 7.93 (2H, dd). 5-188 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 3.03 (3H, d), 3.23-3.36 (2H, m), 4.67 (2H, d), 7.31-7.38 (4H, m), 7.54 (1H, br s), 7.94 (2H, dd). 5-189 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.32 (3H, d), 2.69 (2H, q), 2.84 (3H, s), 4.48 (2H, d), 7.35-7.38 (2H, m), 7.56 (1H, d), 7.65-7.68 (1H, m), 7.92-7.97 (2H, m), 8.45-8.46 (1H, m). 5-190 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.04 (3H, s), 2.32 (3H, s), 2.67 (2H, q), 4.51 (2H, d), 6.08 (1H, s), 7.37 (2H, s), 7.48-7.50 (2H, m), 7.83 (1H, d), 8.39 (1H, d). 5-191 ¹H-NMR (CDCl₃) δ: 1.15-1.24 (6H, m), 2.26 (2H, q), 2.32 (3H, s), 2.67 (3H, q), 4.51 (2H, d), 6.06 (1H, s), 7.37 (2H, s), 7.47-7.49 (2H, m), 7.83 (1H, d), 8.39 (1H, s). 5-192 ¹H-NMR (CDCl₃) δ: 1.22 (3H, tz), 2.33 (3H, s), 2.67 (2H, q), 3.15 (2H, q), 4.57 (2H, d), 6.38 (1H, s), 7.37 (3H, s), 7.49 (1H, d), 7.84 (1H, d), 8.40 (1H, d). 5-193 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 3.94 (3H, s), 7.35 (3H, s), 7.45 (1H, s), 7.54 (1H, d), 7.88 (1H, dd), 8.37 (1H, d). 5-194 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.05 (3H, s), 2.32 (3H, s), 2.67 (2H, q), 4.51 (2H, d), 6.05 (1H, s), 7.36 (2H, s), 7.42 (1H, s), 7.51 (1H, d), 7.84 (1H, d), 8.39 (1H, s). 5-195 ¹H-NMR (CDCl₃) δ: 1.16-1.23 (6H, m), 2.27 (2H, q), 2.33 (3H, s), 2.67 (2H, q), 4.52 (2H, d), 6.04 (1H, s), 7.35 (2H, s), 7.40 (1H, s), 7.50 (1H, d), 7.83 (1H, d), 8.39 (1H, s). 5-196 ¹H-NMR (CDCl₃) δ: 0.77-0.80 (2H, m), 0.99-1.03 (2H, m), 1.21 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 4.54 (2H, d), 6.19 (1H, s), 7.34-7.37 (3H, m), 7.51 (1H, d), 7.85 (1H, d), 8.39 (1H, s). 5-197 ¹H-NMR (CDCl₃) δ: 0.21-0.25 (2H, m), 0.63-0.69 (2H, m), 0.97-1.00 (1H, m), 1.21 (3H, t), 2.21 (2H, d), 2.33 (3H, s), 2.67 (2H, q), 4.54 (2H, d), 6.61 (1H, s), 7.36 (2H, s), 7.44 (1H, s), 7.52 (1H, d), 7.85 (1H, d), 8.40 (1H, d). 5-198 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 3.15 (2H, q), 4.58 (2H, d), 7.36 (2H, s), 7.64-7.67 (1H, m), 7.85 (1H, d), 8.40 (1H, s). 5-199 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 4.81 (2H, d), 7.14 (1H, s), 7.36-7.43 (4H, m), 7.82-7.93 (2H, m), 8.18 (1H, dd), 8.50 (1H, dd). 5-201 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.05 (3H, s), 2.34 (3H, s), 2.69 (2H, q), 4.57 (2H, d), 5.98 (1H, s), 7.30 (1H, br s), 7.36 (2H, s), 7.84-7.87 (2H, m). 5-202 ¹H-NMR (CDCl₃) δ: 1.16-1.24 (6H, m), 2.28 (2H, q), 2.34 (3H, s), 2.69 (2H, q), 4.58 (2H, d), 5.93 (1H, s), 7.30 (1H, d), 7.36 (2H, s), 7.81-7.89 (2H, m). 5-203 ¹H-NMR (CDCl₃) δ: 0.78-0.81 (2H, m), 1.00-1.03 (2H, m), 1.21 (3H, t), 1.38-1.41 (1H, m), 2.34 (3H, s), 2.69 (2H, q), 4.59 (2H, d), 6.09 (1H, s), 7.30 (1H, d), 7.36 (2H, s), 7.82-7.87 (2H, m). 5-204 ¹H-NMR (CDCl₃) δ: 0.20-0.26 (2H, m), 0.61-0.66 (2H, m), 0.97-1.02 (1H, m), 1.21 (3H, t), 2.24 (2H, d), 2.34 (3H, s), 2.70 (2H, q), 4.62 (2H, d), 6.38 (1H, s), 7.30 (1H, d), 7.36 (2H, s), 7.81-7.90 (2H, m). 5-205 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 3.14 (2H, q), 4.63 (2H, d), 6.26 (1H, s), 7.27 (1H, d), 7.37 (2H, s), 7.81-7.87 (2H, m). 5-206 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 4.81 (2H, d), 7.14 (1H, s), 7.36-7.43 (4H, m), 7.84-7.91 (2H, m), 8.18 (1H, dd), 8.50 (1H, dd). 5-211 ¹H-NMR (CDCl₃) δ: 2.04 (3H, s), 2.33 (6H, s), 4.56 (2H, d), 6.07 (1H, s), 7.34 (2H, s), 7.47 (1H, s), 7.54 (1H, d), 7.81 (1H, d), 8.14 (1H, s). 5-212 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 2.26 (2H), 2.32 (6H, s), 4.56 (2H), 6.08 (1H, s), 7.34 (2H, s), 7.51 (1H, d), 7.57 (1H, s), 7.80 (1H, d), 8.13 (1H, s). 5-213 ¹H-NMR (CDCl₃) δ: 1.26 (3H, t), 2.33 (6H, s), 3.14 (2H, q), 4.62 (2H, d), 6.36 (1H, s), 7.34-7.37 (3H, m), 7.52 (1H, d), 7.81 (1H, d), 8.14 (1H, s). 5-219 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 1.92 (3H, s), 2.26 (3H, s), 2.63 (2H, q), 4.47 (2H, d), 6.59 (1H, t), 7.34-7.37 (3H, m), 7.71 (1H, dd), 7.91 (1H, d), 8.39 (1H, s). 5-220 ¹H-NMR (CDCl₃) δ: 1.14-1.24 (6H, m), 2.26 (2H, q), 2.33 (3H, s), 2.67 (2H, q), 4.58 (2H, d), 6.04 (1H, s), 7.37 (2H, s), 7.52-7.53 (2H, m), 7.75 (1H, d), 7.95 (1H, s). 5-221 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.67 (2H, q), 3.14 (2H, q), 4.64 (2H, d), 6.30 (1H, s), 7.34 (1H, s), 7.38 (2H, s), 7.54 (1H, d), 7.76 (1H, d), 7.96 (1H, s). 5-223 ¹H-NMR (CDCl₃) δ: 2.05 (3H, s), 4.52 (2H, d), 5.90 (1H, s), 7.43 (2H, d), 7.66 (2H, s), 7.73 (1H, s), 7.92 (2H, d). 5-224 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.29 (2H, q,), 4.54 (2H, d), 5.84 (1H, s), 7.44 (2H, d), 7.66-7.68 (3H, m), 7.93 (2H, d). 5-225 ¹H-NMR (CDCl₃) δ: 0.21-0.25 (2H, m), 0.61-0.67 (2H, m), 0.97-1.00 (1H, m), 2.24 (2H, d), 4.58 (2H, d), 6.30 (1H, s), 7.45 (2H, d), 7.66-7.68 (3H, m), 7.93 (2H, d, J = 8.2 Hz). 5-226 ¹H-NMR (CDCl₃) δ: 3.16 (2H, q), 4.59 (2H, d), 6.16 (1H, s), 7.43 (2H, d), 7.63 (1H, s), 7.67 (2H, s), 7.93 (2H, d). 5-227 ¹H-NMR (CDCl₃) δ: 1.46 (9H, t), 4.40 (2H, d), 4.98 (1H, s), 7.43 (2H, d), 7.66 (2H, s), 7.69 (1H, s), 7.92 (2H, d). 5-228 ¹H-NMR (CDCl₃) δ: 4.57 (2H, br s), 7.58 (1H, s), 7.66 (2H, s), 7.78-7.82 (2H, m), 7.96 (1H, d). 5-229 ¹H-NMR (CDCl₃) δ: 2.04 (3H, s), 4.58 (2H, d), 6.05 (1H, t), 7.54 (1H, d), 7.67 (2H, s), 7.79 (1H, dd), 7.84 (1H, s), 7.98 (1H, d). 5-230 ¹H-NMR (CDCl₃) δ: 1.17 (3H, t), 2.27 (2H, q), 4.59 (2H, d), 6.01 (1H, br s), 7.54 (1H, d), 7.67 (2H, s), 7.77-7.81 (2H, m), 7.98 (1H, d). 5-231 ¹H-NMR (CDCl₃) δ: 0.75-1.06 (4H, m), 1.39-1.42 (1H, m), 4.61 (2H, d), 6.19 (1H, br s), 7.55 (1H, d), 7.67 (2H, s), 7.72 (1H, s), 7.79 (1H, dd), 7.98 (1H, d). 5-232 ¹H-NMR (acetone-d₆) δ: 3.37 (2H, q), 4.60 (2H, d), 7.62 (1H, d), 7.86 (2H, s), 7.98 (1H, dd), 8.06-8.06 (2H, m), 9.76 (1H, s). 6-1 ¹H-NMR (CDCl₃) δ: 1.26 (3H, t), 2.48 (3H, s), 2.79 (2H, q), 4.40 (2H, s), 7.35 (1H, s), 7.41 (2H, s), 7.55-7.64 (3H, m), 7.80 (1H, d), 8.13-8.15 (1H, m), 8.49-8.52 (1H, m). 6-2 ¹H-NMR (CDCl₃) δ: 1.28 (3H, t), 2.03 (3H, s), 2.47 (3H, s), 2.78 (2H, q), 4.85 (2H, d), 5.93 (1H, s), 7.40-7.42 (4H, m), 7.62-7.64 (2H, m), 7.73 (1H, d), 8.03-8.04 (1H, m), 8.47-8.48 (1H, m). 6-3 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 1.29 (3H, t), 2.26 (2H, q), 2.48 (3H, s), 2.79 (2H, q), 4.91 (2H, d), 5.81 (1H, s), 7.35 (1H, s), 7.41 (2H, s), 7.46 (1H, d), 7.62-7.64 (2H, m), 7.76 (1H, d), 8.06-8.07 (1H, m), 8.48-8.49 (1H, m). 6-4 ¹H-NMR (CDCl₃) δ: 0.76-0.81 (2H, m), 1.04-1.08 (2H, m), 1.29 (3H, t), 1.35-1.38 (1H, m), 2.49 (3H, s), 2.80 (2H, q), 4.96 (2H, d), 5.94 (1H, s), 7.29 (1H, s), 7.42 (2H, s), 7.52 (1H, d), 7.64-7.65 (2H, m), 7.79 (1H, d), 8.09-8.11 (1H, m), 8.49-8.51 (1H, m). 6-5 ¹H-NMR (CDCl₃) δ: 0.17-0.18 (2H, m), 0.56-0.59 (2H, m), 0.92-0.97 (1H, m), 1.29 (2H, t), 2.22 (1H, d), 2.48 (3H, s), 2.80 (2H, q), 4.96 (2H, d), 6.23 (1H, s), 7.35 (1H, s), 7.42 (2H, s), 7.49 (1H, d), 7.63-7.65 (2H, m), 7.78 (1H, d), 8.07-8.09 (1H, m), 8.48-8.49 (1H, m). 6-6 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.45 (3H, s), 2.76 (2H, q), 3.12 (2H, q), 4.58 (2H, d), 6.83 (1H, d), 7.16 (1H, d), 7.41 (2H, s), 7.51 (1H, s), 7.55-7.59 (3H, m), 7.72-7.74 (1H, m), 8.35-8.36 (1H, m). 6-7 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.47 (3H, s), 2.79 (2H, q), 5.15 (2H, d), 7.35-7.38 (1H, m), 7.41 (2H, s), 7.47 (1H, d), 7.54 (1H, d), 7.61-7.66 (1H, m), 7.78 (0H, d), 8.08-8.13 (1H, m), 8.31-8.33 (1H, m), 8.47-8.52 (1H, m), 8.60 (1H, ddd). 7-1 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 2.30 (3H, s), 2.68 (2H, q), 4.06 (2H, s), 7.35 (2H, s), 7.95 (1H, d), 8.26 (1H, d), 8.60 (1H, s), 9.57 (1H, s). 7-2 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.01 (3H, s), 2.33 (3H, s), 2.69 (3H, q), 4.50 (2H, d), 6.50 (1H, t), 7.37 (2H, s), 7.81 (1H, dd), 8.18 (1H, d), 8.56 (1H, d), 9.55 (1H, s). 7-3 ¹H-NMR (CDCl₃) δ: 1.18-1.23 (6H, m), 2.35-2.26 (5H, m), 2.70 (2H, q), 4.56 (2H, d), 5.94 (1H, s), 7.37 (2H, s), 7.84 (1H, dd), 8.25 (1H, d), 8.58 (1H, d), 9.52 (1H, s). 7-5 ¹H-NMR (CDCl₃) δ: 0.62-0.69 (2H, m), 0.63-0.69 (2H, m), 0.96-1.05 (1H, m), 1.18-1.29 (3H, m), 2.26 (2H, d), 2.35 (3H, s), 2.70 (2H, q), 4.61 (2H, d), 6.39 (1H, s), 7.37 (2H, s), 7.85 (1H, d), 8.26 (1H, d), 8.60 (1H, s), 9.52 (1H, s). 7-6 ¹H-NMR (CDCl₃) δ: 1.18-1.28 (3H, m), 2.34 (3H, s), 2.69 (2H, q), 3.19-3.08 (2H, m), 4.59 (2H, d), 6.49 (1H, s), 7.37 (2H, s), 7.82 (1H, dd), 8.21 (1H, d), 8.57 (1H, d), 9.51 (1H, s). 7-19 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 1.47 (9H, s), 2.35 (3H, s), 2.70 (2H, q), 4.43 (2H, d), 5.12 (1H, s), 7.37 (2H, s), 7.84 (1H, dd), 8.25 (1H, d), 8.57 (1H, d), 9.54 (1H, s). 8-2 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.08 (3H, s), 2.34 (3H, s), 2.69 (2H, q), 4.64 (2H, d), 6.71 (1H, s), 7.38 (2H, s), 7.42 (1H, d), 7.62 (1H, s), 8.22 (1H, dd), 9.08 (1H, d). 8-3 ¹H-NMR (CDCl₃) δ: 1.18-1.22 (6H, m), 2.28-2.36 (5H, m), 2.69 (2H, q), 4.63 (2H, d), 6.68 (1H, s), 7.38 (2H, s), 7.42 (1H, s), 7.71 (1H, s), 8.21 (1H, dd), 9.09 (1H, d). 8-6 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 3.20 (3H, q), 4.71 (2H, d), 7.13 (1H, s), 7.40-7.43 (4H, m), 8.24 (1H, dd), 9.08 (1H, s). 8-19 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 1.44 (9H, s), 2.30 (3H, s), 2.67 (2H, q), 4.50 (2H, d), 5.59 (1H, s), 7.38-7.40 (3H, m), 7.90 (1H, s), 8.21 (1H, d), 9.08 (1H, s). 9-1 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 1.45 (3H, d), 2.27-2.33 (5H, m), 2.65 (2H, q), 4.29-4.22 (1H, m), 7.35 (2H, s), 7.50 (2H, d), 7.60 (1H, s), 7.89 (2H, d). 9-2 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 1.52 (2H, d), 2.01 (3H, s), 2.33 (3H, s), 2.68 (2H, q), 5.12-5.21 (1H, m), 5.78 (1H, d), 7.36 (2H, s), 7.47-7.44 (3H, m), 7.89 (2H, d). 9-3 ¹H-NMR (CDCl₃) δ: 1.00 (3H, t), 1.10 (3H, t), 1.40 (3H, d), 2.08-2.19 (5H, m), 2.59 (2H, q), 5.00-5.11 (1H, m), 6.67 (1H, d), 7.34-7.28 (4H, m), 7.86 (2H, d), 8.61 (1H, s). 9-5 ¹H-NMR (DMSO-d₆) δ: 0.12-0.16 (2H, m), 0.41-0.45 (2H, m), 0.93-1.00 (1H, m), 1.11 (3H, t), 1.37 (3H, d), 2.01-2.06 (1H, m), 2.27 (3H, s), 2.65 (2H, q), 4.94-4.99 (1H, m), 7.48-7.40 (4H, m), 7.94 (2H, d), 8.25 (1H, d), 9.88 (1H, s). 9-6 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 1.52 (3H, d), 2.30 (3H, s), 2.66 (2H, q), 3.00-3.11 (2H, m), 5.12-5.21 (1H, m), 6.35 (1H, d), 7.36 (2H, s), 7.41 (2H, d), 7.55 (1H, s), 7.86 (2H, d). 9-7 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 1.41-1.46 (12H, m), 2.31 (3H, s), 2.67 (2H, q), 4.81-4.92 (2H, m), 7.36 (2H, s), 7.42 (1H, d), 7.56 (1H, br s), 7.89 (2H, d). 10-2 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 1.84-1.87 (2H, m), 2.06 (3H, s), 2.35 (3H, s), 2.69 (3H, q), 2.95-3.05 (2H, m), 5.55-5.58 (1H, m), 5.67 (1H, s), 7.35-7.39 (3H, m), 7.43 (1H, d), 7.75 (1H, d), 7.81 (1H, s). 10-3 ¹H-NMR (acetone-d₆) δ: 1.09-1.20 (6H, m), 1.84-1.96 (1H, m), 2.23 (2H, q), 2.35 (3H, s), 2.50-2.53 (1H, m), 2.75 (2H, q), 2.91-3.01 (2H, m), 5.47 (1H, d), 7.27 (1H, s), 7.38 (1H, d), 7.45 (2H, s), 7.88 (2H, d), 9.14 (1H, s). 10-5 ¹H-NMR (CDCl₃) δ: 0.18-0.22 (2H, m), 0.54-0.65 (2H, m), 0.92-1.09 (1H, m), 1.22 (3H, t), 1.83-1.89 (1H, m), 2.24 (2H, d), 2.34 (3H, s), 2.70 (2H, q), 2.89-3.11 (2H, m), 5.57-5.60 (2H, m), 6.15 (1H, d), 7.37 (2H, s), 7.40 (1H, dz), 7.52 (1H, s), 7.77 (1H, d), 7.82 (1H, s). 10-6 ¹H-NMR (acetone-d₆) δ: 1.17 (3H, q), 1.92-1.96 (1H, m), 2.35 (3H, s), 2.52-2.63 (1H, m), 2.75 (2H, q), 2.89-3.10 (2H, m), 3.30 (2H, q), 5.49 (1H, q), 7.40 (1H, d), 7.45 (2H, s), 7.82 (1H, d), 7.89-7.91 (2H, m), 9.16 (1H, s). 10-7 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 1.49 (9H, s), 1.81-1.87 (1H, m), 2.33 (3H, s), 2.62-2.68 (3H, m), 2.83-3.07 (2H, m), 4.79 (1H, d), 5.21 (1H, d), 7.36 (2H, s), 7.43 (1H, d), 7.52 (1H, s), 7.76-7.78 (2H, m). 10-10 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 1.83-1.88 (1H, m), 2.25-2.32 (0H, m), 2.63 (3H, s), 2.69 (2H, q), 2.94-3.05 (2H, m), 5.58 (1H, q), 5.69 (1H, d), 7.35 (2H, s), 7.40 (1H, d), 7.45 (1H, s), 7.75 (1H, d), 7.81 (1H, s). 10-22 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 1.88-1.95 (1H, m), 2.17 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 2.99-3.07 (2H, m), 3.29 (3H, s), 5.58 (1H, q), 7.12 (1H, d), 7.38-7.41 (3H, m), 7.77 (1H, d), 7.83 (1H, s). 11-2 ¹H-NMR (CDCl₃) δ: 1.19 (3H, q), 1.47 (9H, s), 1.74-1.94 (4H, m), 2.30 (3H, s), 2.67 (2H, q), 2.77-2.89 (2H, m), 4.81-4.89 (2H, m), 7.35 (2H, s), 7.46 (1H, d), 7.78-7.61 (3H, m). 11-6 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 1.81-2.16 (4H, m), 2.33 (3H, s), 2.68 (2H, q), 2.85-2.91 (2H, m), 3.06-3.17 (2H, m), 5.25-5.32 (1H, m), 6.07 (1H, d), 7.37-7.39 (4H, m), 7.69-7.64 (2H, m). 11-7 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 1.47 (9H, s), 1.75-1.94 (4H, m), 2.30 (3H, s), 2.67 (2H, q), 2.76-2.94 (3H, m), 4.85 (1H, s), 7.35 (2H, s), 7.46 (1H, d), 7.60-7.78 (3H, m). 12-1 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 1.39 (9H, s), 2.28 (3H, s), 2.66 (2H, q), 4.25 (2H, d), 5.67 (1H, t), 7.36 (2H, s), 7.43 (1H, d), 8.00 (1H, dd), 8.13 (1H, s), 8.23 (1H, d), 8.36 (1H, s), 8.46 (1H, s). 12-2 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.36 (3H, s), 2.71 (2H, q), 3.85 (2H, s), 7.39 (2H, s), 7.54 (1H, d), 7.65 (1H, s), 7.95 (1H, dd), 8.17-8.18 (2H, m), 8.64 (1H, s). 12-3 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t, J = 10.6 Hz), 1.99 (3H, s), 2.35 (3H, s), 2.70 (2H, q), 4.40 (2H, d), 6.85 (1H, t), 7.38 (2H, s), 7.50 (1H, d), 8.08-8.11 (2H, m), 8.22 (1H, s), 8.25 (1H, d), 8.49 (1H, s). 12-4 ¹H-NMR (CDCl₃) δ: 1.13 (3H, t), 1.23 (3H, t), 2.22 (2H, q), 2.35 (3H, s), 2.70 (2H, q), 4.42 (2H, d), 6.79 (1H, t), 7.38 (2H, s), 7.50 (1H, d), 7.94 (1H, s), 8.08 (1H, dd), 8.21 (1H, s), 8.24 (1H, d), 8.49 (1H, s). 12-5 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.37 (3H, s), 2.71 (2H, q), 3.68 (3H, s), 4.35 (2H, d), 5.88 (1H, br s), 7.39 (2H, s), 7.50 (1H, d), 7.64 (1H, br s), 8.06 (1H, d), 8.19-8.20 (2H, m), 8.47 (1H, s). 13-1 ¹H-NMR (CDCl₃) δ: 0.96 (3H, t), 1.19 (3H, t), 2.09 (2H, q), 2.31 (3H, s), 2.69 (2H, q), 4.38 (2H, d), 6.52 (1H, dd), 7.17 (1H, t), 7.36 (2H, s), 7.71 (1H, d), 7.76 (1H, d), 7.84 (1H, d), 8.04-8.08 (2H, m), 8.84 (1H, s). 13-2 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 1.91 (3H, s), 2.32 (3H, s), 2.68 (2H, q), 4.37 (2H, d), 6.82 (1H, t), 7.37 (2H, s), 7.84 (1H, d), 8.05-8.09 (2H, m), 8.19 (1H, s), 8.32 (1H, s), 8.52 (1H, s). 13-3 ¹H-NMR (CDCl₃) δ: 0.99 (3H, t), 1.19 (3H, t), 2.12 (4H, q), 2.30 (3H, s), 2.68 (2H, q), 4.37 (2H, d), 6.91 (1H, t), 7.36 (2H, s), 7.77 (1H, d), 8.08 (1H, d), 8.15 (1H, dd), 8.17 (1H, s), 8.51 (1H, s), 8.82 (1H, s). 14-1 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 6.60 (1H, dd), 7.38 (2H, s), 7.74 (1H, s), 7.84 (1H, d), 7.89-7.97 (2H, m), 8.28 (1H, d), 8.36 (1H, d). 14-2 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 2.27 (3H, s), 2.65 (2H, q), 7.38 (2H, s), 7.94 (1H, d), 8.08 (1H, dd), 8.13 (1H, s), 8.37 (1H, d), 8.49 (1H, s), 8.85 (1H, s). A-1 ¹H-NMR (CDCl₃) δ: 2.32 (6H, s), 7.31-7.36 (3H, m), 7.50 (1H, s), 8.20-8.11 (2H, m). A-2 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 7.29-7.38 (4H, m), 7.67 (1H, br s), 7.78 (1H, dd). A-3 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 7.22-7.36 (4H, m), 7.81 (1H, br s), 8.00 (1H, d). A-4 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 2.27 (3H, s), 2.64 (2H, q), 7.21 (1H, t), 7.36 (2H, s), 7.61 (1H, s), 7.82-7.84 (1H, m), 8.14 (1H, dd). A-5 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.31 (3H, s), 2.66 (2H, q), 7.14 (1H, s), 7.33 (1H, d), 7.38 (2H, s), 7.62 (1H, s), 8.14 (1H, dd), 8.20 (1H, d). B-1 ¹H-NMR (CDCl₃) δ: 2.39 (6H, s), 7.16-7.09 (1H, m), 7.24 (1H, dd), 7.37 (2H, s), 7.60 (1H, s), 7.87 (1H, dd). B-2 ¹H-NMR (CDCl₃) δ: 2.38 (6H, s), 7.14 (1H, s), 7.39-7.33 (3H, m), 7.50 (1H, dd), 7.73 (1H, dd). B-3 ¹H-NMR (CDCl₃) δ: 2.46 (6H, s), 7.20 (1H, s), 7.38 (2H, s), 7.44-7.50 (1H, m), 7.73 (1H, dd), 7.85 (1H, dd). D-1 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.34 (3H, s), 2.70 (2H, q), 7.37 (2H, s), 8.06 (1H, dd), 8.19 (1H, dd), 8.71 (1H, dd), 9.39 (1H, s). E-1 ¹H-NMR (CDCl₃) δ: 1.28 (3H, t), 2.46 (3H, s), 2.77 (2H, q), 7.19 (1H, dd), 7.32 (1H, s), 7.41 (2H, s), 7.64-7.67 (2H, m), 7.80 (1H, dd), 8.18-8.22 (1H, m), 8.47-8.50 (1H, m). F-1 ¹H-NMR (CDCl₃) δ: 2.34 (6H, s), 4.65 (2H, s), 7.36 (2H, s), 7.43 (1H, s), 7.54 (2H, d), 7.92 (2H, d). F-2 ¹H-NMR (CDCl₃) δ: 2.31 (6H, s), 4.92 (2H, s), 7.33 (2H, s), 7.44 (1H, s), 7.56 (2H, d), 7.72-7.89 (6H, m). F-3 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, s), 2.69 (2H, q), 4.65 (2H, s), 7.37 (2H, s), 7.41 (1H, s), 7.55 (2H, d), 7.92 (2H, d). F-4 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 2.31 (3H, s), 2.66 (2H, q), 4.93 (2H, s), 7.35 (2H, s), 7.37 (1H, s), 7.57 (2H, d), 7.75-7.72 (2H, m), 7.89-7.85 (4H, m). F-5 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.76 (3H, s), 7.37 (2H, s), 7.43 (1H, s), 7.64 (1H, d), 7.80 (1H, dd), 7.96 (1H, d). F-6 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.32 (3H, s), 2.66 (2H, q), 5.06 (2H, s), 7.37 (3H, d), 7.76-7.78 (4H, m), 7.87-7.91 (3H, m), 7.96 (1H, d). F-7 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.31 (3H, s), 2.66 (2H, q), 4.75 (2H, s), 7.37 (2H, s), 7.48 (1H, s), 7.63 (1H, d), 7.84 (1H, dd), 8.14 (1H, d). F-8 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.31 (3H, s), 2.66 (2H, q), 5.04 (2H, s), 7.29-7.36 (4H, m), 7.75-7.80 (3H, m), 7.90-7.93 (2H, m), 8.15 (1H, d). F-9 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.32 (3H, s), 2.66 (2H, q), 5.37 (2H, s), 7.37 (2H, s), 7.45 (1H, d), 7.60 (1H, s), 7.82-7.79 (2H, m), 7.93-7.91 (2H, m), 8.12 (1H, dd), 8.64 (1H, d, J = 1.6 Hz). F-14 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.32 (3H, s), 2.67 (2H, q), 4.76 (2H, s), 7.36 (2H, s), 7.46 (1H, s), 7.64 (1H, d), 7.80 (1H, dd), 7.96 (1H, d). F-15 ¹H-NMR (CDCl₃) δ: 1.17-1.22 (3H, m), 2.31 (3H, s), 2.65 (2H, q), 5.06 (2H, s), 7.36-7.39 (4H, m), 7.72-7.97 (6H, m). F-16 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 2.31 (3H, s), 2.65 (2H, q), 5.02 (2H, s), 7.31-7.43 (4H, m), 7.74-7.94 (5H, m), 8.15 (1H, d). F-17 ¹H-NMR (CDCl₃) δ: 1.19 (3H, t), 2.31 (3H, s), 2.65 (2H, q), 5.04 (2H, s), 7.29-7.37 (4H, m), 7.75-7.82 (3H, m), 7.86-7.91 (3H, m), 8.15 (1H, d). G-1 ¹H-NMR (CDCl₃) δ: 1.25 (2H, t), 2.45 (3H, s), 2.77 (2H, q), 5.07 (2H, d), 7.41 (2H, s), 7.55-7.75 (6H, m), 8.22 (1H, d), 8.45 (1H, d). G-2 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.46 (3H, s), 2.77 (2H, q), 5.36 (2H, s), 7.38 (2H, s), 7.59-7.88 (9H, m), 8.41 (1H, d), 8.47 (1H, d). H-1 ¹H-NMR (CDCl₃) δ: 1.22-1.22 (3H, m), 2.34 (3H, s), 2.65-2.73 (5H, m), 7.38 (2H, s), 7.52 (1H, s), 8.00 (2H, d), 8.09 (2H, d). H-2 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.33-2.35 (6H, m), 2.70 (3H, q), 7.43-7.38 (4H, m), 7.79 (2H, d), 7.93 (2H, d). I-1 ¹H-NMR (CDCl₃) δ: 2.36 (6H, s), 7.38 (2H, s), 7.56 (1H, dd), 7.65 (1H, dd), 7.92 (1H, d), 8.30 (1H, dd). I-2 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.27 (3H, s), 2.68 (1H, q), 7.39 (2H, s), 7.47 (1H, s), 7.81 (2H, d), 8.02 (2H, d). I-3 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 7.39 (2H, s), 7.56 (1H, dd), 7.66 (1H, dd), 7.93 (1H, d), 8.31 (1H, dd). I-4 ¹H-NMR (CDCl₃) δ: 1.25 (3H, t), 2.40 (3H, s), 2.74 (2H, q), 7.40 (2H, s), 7.50 (1H, s), 7.70 (1H, dd), 7.81 (1H, d), 7.91 (1H, d). I-5 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.65 (3H, s), 2.68 (2H, q), 7.38 (2H, s), 7.47 (1H, s), 7.74 (1H, d), 7.78 (1H, d), 7.88 (1H, s). I-6 ¹H-NMR (acetone-d₆) δ: 1.17 (3H, t), 2.33 (3H, s), 2.73 (2H, q), 7.56 (1H, s), 7.58 (1H, s), 7.97 (2H, d), 8.21 (2H, d), 9.38 (1H, s). J-1 ¹H-NMR (CDCl₃) δ: 1.24 (3H, t), 2.35 (3H, s), 2.67 (2H, t), 7.40 (2H, s), 7.50 (1H, s), 7.88 (1H, d), 8.40 (1H, dd), 9.22 (1H, d). K-1 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.34 (3H, t), 2.70 (2H, q), 7.39 (2H, s), 8.23 (1H, dd), 8.44 (1H, dd), 8.94 (1H, dd), 9.42 (1H, s). L-1 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.36 (3H, s), 2.70 (2H, q), 2.78-2.80 (2H, m), 3.24-3.26 (2H, m), 7.39 (2H, s), 7.61 (1H, s), 7.87 (2H, s), 8.06 (1H, s). L-2 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.70 (2H, q), 3.03-3.05 (2H, m), 3.15-3.18 (2H, m), 7.38 (2H, s), 7.41 (1H, s), 7.78 (2H, s), 7.90 (1H, s). M-1 ¹H-NMR (CDCl₃) δ: 1.28-1.20 (5H, m), 2.35 (3H, s), 2.66-2.75 (4H, m), 3.07 (2H, t), 7.38 (2H, s), 7.49 (1H, s), 7.78 (1H, d), 7.85 (1H, s), 8.16 (1H, d). M-2 ¹H-NMR (DMSO-d₆) δ: 1.11 (3H, t), 1.74-1.82 (2H, m), 2.27 (3H, s), 2.62-2.72 (4H, m), 2.81 (2H, q), 7.40 (1H, s), 7.45 (1H, s), 7.79-7.82 (2H, m), 7.99 (1H, d), 9.93 (1H, s), 11.35 (1H, s). 5-119 ¹H-NMR (CDCl₃) δ: 3.97 (2H, s), 7.49 (2H, d), 7.86 (2H, s), 7.94 (2H, d). 5-120 ¹H-NMR (CDCl₃) δ: 2.07 (3H, s), 4.53 (2H, d), 5.89 (1H, s), 7.44 (2H, d), 7.71 (1H, s), 7.87 (2H, s), 7.93 (2H, d). 5-121 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.29 (2H, q), 4.54 (2H, d), 5.87 (1H, s), 7.43 (2H, d), 7.73 (1H, s), 7.87 (2H, s), 7.93 (2H, d). 5-123 ¹H-NMR (CDCl₃) δ: 0.22-0.24 (2H, m), 0.63-0.67 (2H, m), 0.99-1.02 (1H, m), 2.25 (2H, d), 4.58 (2H, d), 6.31 (1H, s), 7.46 (2H, d), 7.69 (1H, s), 7.87 (2H, s), 7.94 (2H, d). 5-124 ¹H-NMR (CDCl₃) δ: 3.20 (2H, q), 4.59 (2H, d), 6.25 (1H, s), 7.43 (2H, d), 7.68 (1H, s), 7.87 (2H, s), 7.93 (2H, d). 5-234 ¹H-NMR (CDCl₃) δ: 2.03 (3H, s), 4.57 (2H, d), 6.14 (1H, s), 7.50 (1H, dd), 7.79 (1H, dd), 7.87 (2H, s), 7.98 (1H, d). 5-241 ¹H-NMR (CDCl₃) δ: 4.57 (2H, s), 7.67-7.88 (6H, m). 5-242 ¹H-NMR (CDCl₃) δ: 2.04 (3H, s), 4.57 (2H, d), 6.08 (1H, t), 7.53 (1H, d), 7.65 (2H, s), 7.79 (1H, dd), 7.88 (1H, s), 7.98 (1H, d). 5-243 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 2.28 (2H, q), 4.59 (2H, d), 5.99 (1H, s), 7.56 (1H, d), 7.65 (2H, s), 7.69 (1H, s), 7.79 (1H, dd), 7.98 (1H, d). 5-244 ¹H-NMR (CDCl₃) δ: 3.14 (2H, dd), 4.65 (2H, d), 6.29 (1H, s), 7.55 (1H, d), 7.61 (1H, s), 7.66 (2H, s), 7.81 (1H, d), 7.99 (1H, s). 5-285 ¹H-NMR (CDCl₃) δ: 4.56 (2H, s), 6.58 (1H, t), 7.46 (1H, d), 7.67-7.79 (4H, m), 7.94 (1H, d). 5-286 ¹H-NMR (CDCl₃) δ: 2.04 (3H, s), 4.58 (2H, d), 6.06 (1H, br s), 6.57 (1H, t), 7.50 (1H, s), 7.54 (1H, d), 7.75-7.78 (3H, m), 7.96 (1H, d). 5-287 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 2.28 (2H, q), 4.59 (2H, d), 6.00 (1H, d), 6.58 (1H, t), 7.50-7.57 (2H, m), 7.71-7.76 (3H, m), 7.96 (1H, d). 5-288 ¹H-NMR (CDCl₃) δ: 3.14 (2H, q), 4.64 (2H, d), 6.30 (1H, s), 6.58 (1H, t), 7.52-7.55 (3H, m), 7.77-7.79 (2H, m), 7.97 (1H, d). 5-293 ¹H-NMR (CDCl₃) δ: 1.70 (2H, s), 2.39 (3H, s), 4.03 (2H, s), 6.51 (1H, t), 7.32 (1H, s), 7.42 (1H, s), 7.59 (1H, d), 7.67 (1H, s), 7.78 (1H, dd), 7.92 (1H, d). 5-294 ¹H-NMR (CDCl₃) δ: 2.04 (3H, s), 2.38 (3H, s), 4.57 (2H, d), 6.06 (1H, s), 6.51 (1H, t), 7.32 (1H, s), 7.42 (1H, s), 7.53 (1H, d), 7.73-7.76 (2H, m), 7.94 (1H, d). 5-295 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 2.27 (2H, q), 2.38 (3H, s), 4.57 (2H, d), 6.05 (1H, t), 6.51 (1H, t), 7.32 (1H, s), 7.42 (1H, s), 7.51 (1H, d), 7.74 (1H, dd), 7.80 (1H, s), 7.94 (1H, d). 5-296 ¹H-NMR (CDCl₃) δ: 2.38 (3H, s), 3.14 (2H, q), 4.63 (2H, d), 6.40 (1H, s), 6.52 (1H, t), 7.32 (1H, s), 7.43 (1H, s), 7.52 (1H, d), 7.66 (1H, s), 7.75 (1H, d), 7.95 (1H, d). 5-305 ¹H-NMR (CDCl₃) δ: 4.02 (1H, s), 4.56 (1H, s), 6.58 (2H, t), 7.46 (1H, s), 7.57-7.68 (3H, m), 7.77-7.81 (1H, m), 7.93 (1H, d). 5-306 ¹H-NMR (CDCl₃) δ: 2.05 (3H, d), 4.57 (2H, d), 6.09 (1H, s), 6.58 (1H, t), 7.46 (1H, s), 7.53 (1H, d), 7.63 (1H, s), 7.77 (1H, dd), 7.84 (1H, s), 7.95 (1H, d). 5-307 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 2.26 (2H, q), 4.57 (2H, d), 6.07 (1H, t), 6.58 (1H, t), 7.46 (1H, s), 7.51 (1H, d), 7.63 (1H, s), 7.77 (1H, dd), 7.87 (1H, s), 7.95 (1H, d). 5-308 ¹H-NMR (CDCl₃) δ: 3.14 (2H, q), 4.64 (2H, d), 6.58 (1H, t), 7.47 (1H, s), 7.54 (1H, d), 7.58 (1H, s), 7.64 (1H, s), 7.78 (1H, d), 7.97 (1H, s). 5-310 1H-NMR (CDCl3) δ: 2.04 (3H, d), 4.57 (2H, d), 6.08 (1H, d), 6.57 (1H, t), 7.45 (1H, s), 7.53 (1H, d), 7.62 (1H, s), 7.77 (1H, dd), 7.80 (1H, s), 7.95 (1H, d). 5-311 1H-NMR (CDCl3) δ: 1.18 (3H, t), 2.28 (2H, q), 4.59 (2H, d), 5.98 (1H, s), 6.57 (1H, t), 7.45 (1H, s), 7.56 (1H, d), 7.60 (1H, s), 7.62 (1H, s), 7.76 (1H, t), 7.95 (1H, d). 5-312 1H-NMR (CDCl3) δ: 3.13 (2H, t), 4.65 (2H, d), 6.29 (1H, d), 6.57 (1H, t), 7.46 (1H, s), 7.54-7.57 (2H, m), 7.63 (1H, s), 7.78 (1H, d), 7.97 (1H, s). 5-317 ¹H-NMR (CDCl₃) δ: 1.46 (9H, s), 4.47 (2H, d), 5.09 (1H, s), 7.55 (1H, d), 7.63 (1H, s), 7.67 (2H, s), 7.82 (1H, dd), 7.96 (1H, d). 5-318 ¹H-NMR (CDCl₃) δ: 0.76-1.09 (4H, m), 1.61 (1H, td), 2.33 (3H, s), 2.67 (2H, q), 4.60 (2H, d), 6.21 (1H, s), 7.38 (2H, s), 7.46 (1H, s), 7.54 (1H, d), 7.75 (1H, d), 7.96 (1H, s). 5-322 ¹H-NMR (CDCl₃) δ: 2.06 (3H, s), 4.52 (2H, d), 5.95 (1H, s), 7.42 (2H, d), 7.65 (2H, s), 7.79 (1H, s), 7.92 (2H, d). 5-323 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.29 (2H, q), 4.54 (2H, d), 5.85 (1H, s), 7.44 (2H, d), 7.65 (2H, s), 7.70 (1H, s), 7.92 (2H, d). 5-324 ¹H-NMR (CDCl₃) δ: 3.22 (2H, q), 4.58 (2H, d), 6.26 (1H, s), 7.42 (2H, d), 7.65 (2H, s), 7.69 (1H, s), 7.91 (2H, d). 5-325 ¹H-NMR (CDCl₃) δ: 0.21-0.25 (2H, m), 0.62-0.64 (2H, m), 0.98-1.02 (1H, m), 2.25 (2H, d, J = 7.1 Hz), 4.58 (2H, d), 6.30 (1H, s), 7.45 (2H, d), 7.65 (2H, s), 7.68 (1H, s), 7.93 (2H, d). 5-326 ¹H-NMR (CDCl₃) δ: 0.77-0.81 (2H, m), 1.02 (2H, dd), 1.39-1.41 (1H, m), 4.54 (2H, d), 6.06 (1H, s), 7.44 (2H, d), 7.65 (2H, s), 7.73 (1H, s), 7.92 (2H, d). 5-327 ¹H-NMR (CDCl₃) δ: 2.14 (3H, s), 3.28 (2H, s), 4.59 (2H, d), 7.46 (2H, d), 7.65 (3H, br s), 7.94 (2H, d). 5-328 ¹H-NMR (CDCl₃) δ: 1.47 (9H, s), 4.40 (2H, d), 7.43 (2H, d), 7.65 (3H, br s), 7.92 (2H, d). 5-329 ¹H-NMR (CDCl₃) δ: 1.44 (9H, s), 4.46 (2H, d), 5.14 (1H, s), 7.52 (1H, d), 7.65 (3H, br s), 7.82 (1H, d), 7.97 (1H, d). 5-330 ¹H-NMR (CDCl₃) δ: 0.22 (2H, d), 0.63-0.66 (2H, m), 0.96-0.98 (1H, m), 2.21 (2H, d), 4.62 (2H), 6.51 (1H, s), 7.57 (1H, d), 7.65 (2H, s), 7.68 (1H, s), 7.80 (1H, dd), 7.99 (1H, d). 5-331 ¹H-NMR (CDCl₃) δ: 2.14 (3H, s), 3.25 (2H, s), 4.64 (2H, d), 7.57 (1H, d), 7.63 (1H, s), 7.66 (2H, s), 7.81 (1H, dd), 7.99 (1H, d). 5-333 ¹H-NMR (CDCl₃) δ: 2.02 (3H, s), 2.39 (3H, s), 4.50 (2H, d), 6.07 (1H, s), 7.40 (2H, d), 7.43 (1H, s), 7.56 (1H, s), 7.90 (2H, d). 5-334 ¹H-NMR (CDCl₃) δ: 1.20 (3H, t), 2.28 (2H, q), 2.40 (3H, s), 4.53 (2H, d), 5.90 (1H, s), 7.41-7.44 (3H, m), 7.56 (1H, s), 7.76 (1H, s), 7.91 (2H, d). 5-335 ¹H-NMR (CDCl₃) δ: 2.35 (3H, s), 3.09 (2H, q), 4.51 (2H, d), 6.64 (1H, s), 7.33 (2H, d), 7.41 (1H, s), 7.54 (1H, s), 7.83 (2H, d). 5-336 ¹H-NMR (CDCl₃) δ: 0.18-0.26 (2H, m), 0.62 (2H, m), 0.98-1.02 (1H, m), 2.25 (2H, d), 2.41 (3H, s), 4.58 (2H, d), 6.31 (1H, s), 7.44-7.46 (3H, m), 7.56 (1H, s), 7.70 (1H, s), 7.92 (2H, d). 5-337 ¹H-NMR (CDCl₃) δ: 2.11 (3H, s), 2.37 (3H, s), 3.24 (2H, s), 4.55 (2H, d), 7.32 (1H, s), 7.41-7.42 (3H, m), 7.54 (1H, s), 7.79 (1H, s), 7.90 (2H, d). 5-338 ¹H-NMR (CDCl₃) δ: 0.68-1.02 (4H, m), 1.34-1.42 (1H, m), 2.35 (3H, s), 4.47 (2H, d), 6.39 (1H, s), 7.33 (2H, d), 7.40 (1H, s), 7.53 (1H, s), 7.84-7.87 (2H, m). 5-339 ¹H-NMR (CDCl₃) δ: 1.47 (9H, s), 2.40 (3H, s), 4.40 (2H, d), 7.42-7.44 (3H, m), 7.56 (1H, s), 7.77 (1H, s), 7.92 (2H, d). 5-340 ¹H-NMR (CDCl₃) δ: 0.21-0.22 (2H, m), 0.61-0.67 (2H, m), 0.93-0.99 (1H, m), 2.20 (2H, d), 2.39 (3H, s), 4.61 (2H, d), 6.52 (1H, t), 6.53 (1H, s), 7.32 (1H, s), 7.42 (1H, s), 7.53 (1H, d), 7.74-7.77 (2H, m), 7.95 (1H, d). 5-341 ¹H-NMR (CDCl₃) δ: 0.75-1.09 (4H, m), 1.59-1.63 (1H, m), 2.39 (3H, s), 4.60 (2H, d), 6.19 (1H, s), 6.52 (1H, t), 7.32 (1H, s), 7.42 (1H, s), 7.54 (1H, d), 7.66 (1H, s), 7.75 (1H, t), 7.94 (1H, d). 5-342 ¹H-NMR (CDCl₃) δ: 1.46 (9H, s), 2.39 (3H, s), 4.46 (2H, d), 5.11 (1H, s), 6.51 (1H, t), 7.32 (1H, s), 7.42 (1H, s), 7.52 (1H, d), 7.67 (1H, s), 7.77 (1H, d), 7.93 (1H, d). 5-344 1H-NMR (CDCl3) δ: 2.07 (3H, s), 2.42 (3H, s), 4.51 (2H, d), 5.70 (1H, s), 7.38 (1H, d), 7.65-7.66 (3H, m), 7.75-7.77 (2H, m). 5-345 ¹H-NMR (CDCl₃) δ: 1.21 (3H, t), 2.29 (3H, q), 2.42 (3H, s), 4.51 (2H, d), 5.68 (1H, s), 7.37 (1H, d), 7.64-7.68 (3H, m), 7.74-7.76 (2H, m). 5-346 ¹H-NMR (CDCl₃) δ: 2.42 (3H, s), 3.16 (2H, q), 4.57 (2H, d), 6.00 (1H, s), 7.37 (1H, d), 7.63 (1H, s), 7.67 (2H, s), 7.76 (1H, d), 7.79 (1H, s). 5-347 ¹H-NMR (CDCl₃) δ: 1.47 (9H, s), 2.39 (3H, s), 4.37 (2H, d), 4.90 (1H, s), 7.39 (1H, d), 7.66 (3H, s), 7.76 (2H, d). 5-348 ¹H-NMR (CDCl₃) δ: 4.61 (2H, d), 7.41 (2H, d), 7.65 (3H, s), 7.90 (2H, d). 5-349 ¹H-NMR (CDCl₃) δ: 1.17 (3H, t), 2.27 (3H, s), 2.64 (2H, q), 4.63 (2H, d), 7.36 (2H, s), 7.43 (1H, d), 7.79 (1H, d), 8.13 (1H, s). 5-440 ¹H-NMR (CDCl₃) δ: 1.46 (9H, s), 4.40 (2H, d), 4.98 (1H, s), 7.43 (2H, d), 7.72 (1H, s), 7.86 (2H, s), 7.93 (2H, d). 5-441 ¹H-NMR (CDCl₃) δ: 1.16 (3H, t), 1.62-1.67 (1H, m), 1.99-2.08 (1H, m), 2.25 (3H, s), 2.32-2.36 (1H, m), 2.63 (2H, q), 4.50-4.52 (2H, m), 6.83 (1H, d), 7.31-7.33 (3H, m), 7.68 (1H, dd), 7.95 (1H, s), 8.04 (1H, d). 5-442 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.34 (3H, s), 2.68 (2H, q), 3.43 (2H, s), 4.63 (2H, d), 6.70 (1H, s), 7.36-7.39 (3H, m), 7.55 (1H, d), 7.82 (1H, d), 8.16 (1H, s). 5-443 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 4.03 (2H, s), 7.45 (1H, s), 7.58-7.60 (2H, m), 7.72 (1H, s), 7.82 (1H, dd), 7.95 (1H, d). 5-444 ¹H-NMR (CDCl₃) δ: 2.17 (3H, s), 2.38 (3H, s), 4.56 (2H, d), 6.15 (1H, t), 7.44 (1H, s), 7.51 (1H, d), 7.57 (1H, s), 7.78 (1H, dd), 7.92 (1H, s), 7.97 (1H, d). 5-445 ¹H-NMR (CDCl₃) δ: 1.18 (3H, t), 2.28 (2H, q), 2.40 (3H, s), 4.59 (2H, d), 5.98 (1H, s), 7.44 (1H, s), 7.54-7.57 (2H, m), 7.67 (1H, s), 7.78 (1H, dd), 7.97 (1H, d). 5-446 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 3.14 (2H, q), 4.64 (2H, d), 6.28 (1H, s), 7.45 (1H, s), 7.56-7.60 (2H, m), 7.79 (1H, d), 7.98 (1H, s). 5-447 ¹H-NMR (CDCl₃) δ: 1.46 (9H, s), 2.40 (3H, s), 4.47 (2H, d), 5.09 (1H, s), 7.44 (1H, s), 7.54-7.56 (2H, m), 7.67 (1H, s), 7.80 (1H, dd), 7.95 (1H, d). 5-448 ¹H-NMR (CDCl₃) δ: 1.45 (9H, s), 4.45 (2H, d), 5.14 (1H, s), 6.58 (1H, t), 7.46 (1H, s), 7.51 (1H, d), 7.63 (1H, s), 7.79 (1H, dd), 7.94 (1H, d). 5-449 ¹H-NMR (CDCl₃) δ: 1.47 (9H, s), 4.47 (2H, d), 5.10 (1H, s), 6.58 (1H, t), 7.52-7.57 (3H, m), 7.78-7.81 (2H, m), 7.94 (1H, d). 5-450 ¹H-NMR (CDCl₃) δ: 0.19-0.22 (2H, m), 0.58-0.64 (2H, m), 0.97-1.04 (1H, m), 2.21 (2H, d), 4.62 (2H, d), 6.54 (1H, s), 6.58 (2H, t), 7.46 (1H, s), 7.55 (1H, d), 7.63 (1H, s), 7.73 (1H, s), 7.78 (1H, dd), 7.96 (1H, d). 5-451 ¹H-NMR (CDCl₃) δ: 1.46 (9H, s), 4.47 (2H, d), 5.10 (1H, s), 7.54 (1H, d), 7.82 (1H, d), 7.87 (2H, s), 7.97 (1H, d). 5-452 1H-NMR (CDCl3) δ: 3.16 (2H, q), 4.59 (2H, d), 6.19 (1H, s), 6.58 (1H, t), 7.42-7.44 (3H, m), 7.61-7.62 (2H, m), 7.90 (2H, d). 5-453 1H-NMR (CDCl3) δ: 1.47 (9H, s), 4.39 (2H, d), 5.01 (1H, s), 6.58 (1H, t), 7.43 (3H, dq), 7.62 (1H, s), 7.71 (1H, s), 7.90 (2H, d). 5-454 1H-NMR (CDCl3) δ: 0.77-1.07 (4H, m), 1.60-1.63 (1H, m), 4.61 (2H, d), 6.17 (1H, s), 6.57 (1H, t), 7.46 (1H, s), 7.56 (1H, d), 7.60 (1H, s), 7.63 (1H, s), 7.77 (1H, d), 7.95 (1H, d). 5-455 1H-NMR (CDCl3) δ: 0.20-0.21 (2H, m), 0.57-0.66 (2H, m), 0.98 (1H, s), 2.22 (2H, d), 4.62 (2H, d), 6.52 (1H, s), 6.57 (1H, t), 7.45 (1H, s), 7.56 (1H, d), 7.63 (1H, s), 7.65 (1H, s), 7.77 (1H, dd), 7.96 (1H, d). 5-456 1H-NMR (CDCl3) δ: 1.46 (9H, s), 4.46 (2H, d), 5.09 (1H, s), 6.58 (1H, t), 7.45 (1H, s), 7.54 (1H, d), 7.62 (2H, s), 7.78 (1H, dd), 7.93 (1H, d). A-6 ¹H-NMR (CDCl₃) δ: 7.63-7.67 (5H, m), 7.89 (2H, d). A-7 ¹H-NMR (CDCl₃) δ: 7.49 (1H, dd), 7.60 (1H, s), 7.67 (2H, s), 8.00 (1H, d), 8.04 (1H, d). A-8 ¹H-NMR (CDCl₃) δ: 7.64 (1H, s), 7.68 (2H, d), 7.87 (2H, s), 7.90 (2H, d). A-9 ¹H-NMR (CDCl₃) δ: 7.49 (1H, dd), 7.65 (3H, br s), 8.00 (1H, d), 8.03 (1H, d). A-10 ¹H-NMR (CDCl₃) δ: 7.49 (1H, dd), 7.65 (3H, s), 8.00 (1H, d), 8.03 (1H, d). A-11 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 7.45 (1H, s), 7.49 (1H, dd), 7.57-7.60 (2H, m), 8.00 (1H, d), 8.04 (1H, d). N-1 ¹H-NMR (CDCl₃) δ: 7.68 (2H, d), 7.80 (1H, s), 8.13 (2H, d), 8.39 (2H, d). N-2 ¹H-NMR (CDCl₃) δ: 7.69 (2H, s), 8.11 (2H, d), 8.36 (2H, d), 8.58 (1H, br s). N-4 ¹H-NMR (CDCl₃) δ: 2.67 (3H, s), 7.66-7.70 (2H, m), 7.89 (1H, dd), 7.94 (1H, s), 8.05 (1H, d), 8.12 (1H, s). N-7 ¹H-NMR (CDCl₃) δ: 2.42 (3H, s), 7.47 (1H, s), 7.59 (1H, s), 7.82 (1H, s), 8.12 (2H, d), 8.38 (2H, d). N-14 ¹H-NMR (CDCl₃) δ: 7.83 (1H, s), 7.88 (2H, s), 8.13 (1H, d), 8.37 (1H, d). O-1 ¹H-NMR (CDCl₃) δ: 6.72 (2H, d), 7.56 (1H, s), 7.63 (2H, s), 7.78 (2H, d). O-2 ¹H-NMR (CDCl₃) δ: 4.12 (2H, br s), 6.72 (2H, d), 7.55 (1H, s), 7.62 (2H, s), 7.79 (2H, d). O-4 ¹H-NMR (CDCl₃) δ: 4.53 (2H, s), 6.82 (1H, d), 7.52 (1H, s), 7.64 (2H, s), 7.68 (1H, dd), 7.90 (1H, d). O-5 ¹H-NMR (CDCl₃) δ: 4.53 (2H, br s), 6.81 (1H, d), 7.56 (1H, s), 7.63 (2H, s), 7.68 (1H, dd), 7.90 (1H, d). O-7 ¹H-NMR (CDCl₃) δ: 2.23 (3H, s), 4.07 (2H, br s), 6.72 (1H, d), 7.54 (1H, s), 7.64-7.67 (2H, m), 7.70 (1H, s). O-10 ¹H-NMR (CDCl₃) δ: 2.39 (3H, s), 4.11 (2H, br s), 6.72 (2H, d), 7.42 (1H, s), 7.54 (1H, s), 7.57 (1H, s), 7.78 (2H, d). O-23 ¹H-NMR (CDCl₃) δ: 4.11 (2H, s), 6.73 (2H, d), 7.53 (1H, s), 7.78-7.83 (4H, m). O-29 ¹H-NMR (CDCl₃) δ: 4.57 (2H, s), 6.81 (1H, d), 7.55 (1H, s), 7.72 (1H, dd), 7.83 (2H, s), 8.06 (1H, d). O-31 ¹H-NMR (CDCl₃) δ: 2.38 (3H, s), 4.50 (2H, s), 6.82 (1H, d), 7.42 (1H, s), 7.52-7.54 (2H, m), 7.67 (1H, dd), 7.89 (1H, d). I-12 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 6.53 (1H, t), 7.33 (1H, s), 7.44 (1H, s), 7.66 (1H, s), 7.82-7.90 (2H, m), 8.06 (1H, d). I-15 ¹H-NMR (CDCl₃) δ: 6.58 (1H, t), 7.47 (1H, s), 7.65 (1H, s), 7.82-7.93 (3H, m), 8.08 (1H, d). I-16 ¹H-NMR (CDCl₃) δ: 6.57 (1H, t), 7.46 (1H, s), 7.64 (1H, s), 7.82-7.92 (3H, m), 8.07 (1H, d). I-18 ¹H-NMR (CDCl₃) δ: 6.57 (1H, t), 7.51 (1H, s), 7.70 (1H, s), 7.81-7.92 (3H, m), 8.07 (1H, d). I-29 ¹H-NMR (CDCl₃) δ: 2.33 (6H, s), 7.38 (2H, s), 7.48 (1H, s), 7.77-7.80 (3H, m). I-30 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.33 (3H, s), 2.66 (2H, t), 7.39 (2H, s), 7.43 (1H, s), 7.77-7.81 (3H, m). I-31 ¹H-NMR (CDCl₃) δ: 1.23 (3H, t), 2.35 (3H, s), 2.69 (2H, q), 7.39 (2H, s), 7.55 (1H, dd), 7.95 (1H, d), 8.05 (1H, dd). I-32 ¹H-NMR (CDCl₃) δ: 7.67 (2H, s), 7.75 (1H, s), 7.85 (1H, d), 7.93 (1H, dd), 8.09 (1H, d). I-33 ¹H-NMR (CDCl₃) δ: 7.74 (1H, s), 7.84 (2H, d), 7.88 (2H, s), 8.07 (2H, d). I-34 ¹H-NMR (CDCl₃) δ: 7.65 (1H, s), 7.86 (1H, d), 7.89 (2H, s), 7.93 (1H, dd), 8.10 (1H, d). I-35 ¹H-NMR (CDCl₃) δ: 2.40 (3H, s), 7.47 (1H, s), 7.59 (1H, s), 7.70 (1H, s), 7.85 (1H, d), 7.92 (1H, dd), 8.09 (1H, d). I-36 ¹H-NMR (CDCl₃) δ: 1.22 (3H, t), 2.33 (3H, s), 2.67 (2H, q), 7.38 (2H, s), 7.45 (1H, s), 7.83 (1H, d), 7.89 (1H, dd), 8.06 (1H, d). I-37 ¹H-NMR (CDCl₃) δ: 7.84 (1H, d), 7.87 (2H, s), 7.94 (1H, dd), 7.98 (1H, s), 8.11 (1H, d). I-38 ¹H-NMR (CDCl₃) d: 7.69 (2H, s), 7.72 (1H, s), 7.85 (1H, d), 7.93 (1H, dd), 8.09 (1H, d).

The test preparations in Biological test examples 1 to 3 were prepared as follows.

Solvent: 3 parts by weight of dimethylformamide

Emulsifier: 1 part by weight of polyoxyethylene alkyl phenyl ether

To prepare a suitable preparation containing the active compound, 1 part by weight of the active compound was mixed with the above amount of the solvent containing the above amount of the emulsifier, and the resulting mixture was diluted with water to a predetermined concentration.

Biological Test Example 1 Test Against Tobacco Cutworm (Spodoptera litura) Larvae

Leaves of sweet potato were immersed in the test solution at the appropriate concentration, and the leaves were dried in air. The leaves were then placed in a petri dish having a diameter of 9 cm, and ten Spodoptera litura at third instar larvae were released therein. The petri dishes were placed in a temperature-controlled chamber at 25° C. After 2 days and 4 days more sweet potato leaves were added. After 7 days, the number of dead larvae was counted to calculate the insecticidal activity. An insecticidal activity of 100% means that all larvae were killed, whereas an insecticidal activity of 0% means that no larva was killed. In the current test, the results of two petri dishes for each treatment were averaged.

In the biological test example 1, the compounds Nos. 1-3, 1-7, 1-8, 1-9, 1-11, 1-12, 1-17, 1-20, 1-24, 1-27, 1-28, 1-30, 1-31, 1-32, 1-33, 1-34, 1-35, 1-36, 1-37, 1-38, 1-39, 1-40, 1-41, 1-42, 1-43, 1-44, 1-47, 1-49, 1-50, 1-55, 1-56, 1-58, 1-64, 1-69, 1-73, 1-74, 1-75, 1-77, 1-78, 1-79, 1-80, 1-81, 1-89, 1-96, 1-103, 2-2, 4-2, 5-3, 5-7, 5-8, 5-19, 5-21, 5-22, 5-24, 5-28, 5-29, 5-30, 5-31, 5-32, 5-34, 5-35, 5-36, 5-37, 5-38, 5-39, 5-41, 5-45, 5-46, 5-51, 5-52, 5-53, 5-54, 5-55, 5-58, 5-59, 5-61, 5-62, 5-66, 5-67, 5-68, 5-72, 5-76, 5-77, 5-78, 5-79, 5-80, 5-81, 5-82, 5-83, 5-85, 5-86, 5-88, 5-89, 5-91, 5-93, 5-94, 5-96, 5-99, 5-100, 5-101, 5-102, 5-103, 5-106, 5-107, 5-108, 5-110, 5-112, 5-115, 5-116, 5-117, 5-139, 5-142, 5-144, 5-145, 5-146, 5-147, 5-148, 5-149, 5-150, 5-151, 5-152, 5-153, 5-154, 5-155, 5-157, 5-158, 5-159, 5-160, 5-161, 5-174, 5-175, 5-177, 5-178, 5-179, 5-181, 5-182, 5-183, 5-188, 5-189, 5-190, 5-191, 5-192, 5-194, 5-195, 5-196, 5-197, 5-198, 5-201, 5-202, 5-203, 5-204, 5-205, 5-206, 5-211, 5-212, 5-213, 5-219, 5-220, 5-221, 5-225, 5-229, 5-230, 5-231, 5-232, 5-242, 5-243, 5-244, 5-293, 5-294, 5-295, 5-296, 5-318, 5-319, 5-320, 5-322, 5-323, 5-324, 5-325, 5-326, 5-329, 5-330, 5-331, 5-335, 5-336, 5-340, 5-341, 5-349, 6-2, 6-3, 6-4, 6-5, 6-6, 6-7, 7-2, 7-3, 7-5, 7-6, 8-2, 8-6, 9-2, 9-3, 9-5, 9-6, 10-2, 10-3, 10-5, 10-6, 10-10, 10-22, 11-2, 11-6, 12-1, 12-3, 12-4, 12-5, A-3, A-4, A-7, A-8, A-10, I-2, I-3, I-5, I-12, I-24, I-25, I-26, I-27 and I-28 showed an insecticidal activity of 100% at an active compound concentration of 100 ppm.

Biological Test Example 2 Test Against Two-Spotted Spider Mite (Tetranychus Urticae)

50 to 100 adult mites of Tetranychus urticae were inoculated to leaves of kidney bean at two-leaf stage planted in a pot of 6 cm in diameter. After one day, test solution at the appropriate concentration was sprayed thereon in a sufficient amount using a spray gun. After the spraying, the plant pot was placed inside a greenhouse, and after 7 days, the acaricidal activity was calculated. An acaricidal activity of 100% means that all mites were killed, whereas an acaricidal activity of 0% means that no mite was killed. In the biological test example 2, the compound Nos. 1-11, 1-12, 1-27, 1-31, 1-32, 1-35, 1-36, 1-39, 1-41, 1-46, 1-49, 1-55, 1-73, 1-74, 1-75, 1-78, 1-80, 1-81, 1-89, 1-99, 5-28, 5-29, 5-30, 5-32, 5-33, 5-36, 5-40, 5-41, 5-44, 5-58, 5-61, 5-62, 5-72, 5-77, 5-78, 5-80, 5-81, 5-82, 5-85, 5-86, 5-88, 5-89, 5-91, 5-92, 5-93, 5-94, 5-102, 5-103, 5-110, 5-112, 5-147, 5-148, 5-150, 5-151, 5-153, 5-154, 5-155, 5-157, 5-175, 5-179, 5-186, 5-187, 5-188, 5-192, 5-213, 5-219, 5-220, 5-221, 5-224, 5-225, 5-242, 5-243, 5-244, 5-294, 5-295, 5-296, 5-319, 5-320, 5-331, 5-333, 5-340, 5-341, 9-2, 9-3, 10-3, 10-5, 10-6, 10-10, 11-2 and I-12 showed an acaricidal activity of 100% at an active compound concentration of 100 ppm.

Biological Test Example 3 Test Against Cucurbit Leaf Beetle (Aulacophora Femoralis)

Leaves of cucumber were immersed in the test solution at the appropriate concentration, and the leaves were dried in air. The leaves were then put in a plastic cup containing sterilized black soil and five Aulacophora femoralis at second instar larvae were released in the cup. The cups were placed in a temperature-controlled chamber at 25° C. After 7 days, the number of dead larvae was counted, and thus the insecticidal activity was calculated. An insecticidal activity of 100% means that all larvae were killed, whereas an insecticidal activity of 0% means that no larva was killed.

In the biological test example 3, the compounds Nos. 1-3, 1-5, 1-6, 1-7, 1-8, 1-11, 1-12, 1-25, 1-31, 1-32, 1-34, 1-37, 1-47, 1-49, 1-55, 1-56, 1-58, 1-67, 1-68, 1-69, 1-73, 1-77, 1-78, 1-79, 1-80, 1-101, 2-2, 4-2, 5-8, 5-21, 5-22, 5-30, 5-34, 5-35, 5-36, 5-40, 5-41, 5-44, 5-45, 5-46, 5-51, 5-58, 5-59, 5-61, 5-62, 5-65, 5-77, 5-78, 5-79, 5-81, 5-82, 5-85, 5-86, 5-89, 5-93, 5-96, 5-100, 5-102, 5-103, 5-127, 5-139, 5-142, 5-144, 5-145, 5-148, 5-150, 5-151, 5-152, 5-154, 5-155, 5-157, 5-161, 5-174, 5-175, 5-177, 5-178, 5-179, 5-181, 5-183, 5-198, 5-201, 5-202, 5-203, 5-204, 5-205, 5-206, 5-211, 5-212, 5-213, 5-219, 5-220, 5-221, 5-224, 5-225, 5-226, 5-229, 5-231, 5-242, 5-243, 5-244, 5-294, 5-295, 5-296, 5-320, 5-323, 5-324, 5-326, 5-331, 5-341, 6-6, 6-7, 7-2, 7-3, 7-5, 8-2, 9-2, 9-3, 9-6, 10-3, 10-6, 10-22, I-5, I-12, I-24, I-26 and I-27 showed an insecticidal activity of 100% at an active compound concentration of 100 ppm.

Biological Test Example 4 Boophilus Microplus—Test (Injection)

Solvent: dimethyl sulfoxide

To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 ml solvent, and the concentrate is diluted with solvent to the desired concentration. Five adult engorged female ticks (Boophilus microplus) are injected with 1 ml compound solution into the abdomen. Ticks are transferred into replica plates and incubated in a climate chamber for a period of time. Egg deposition of fertile eggs is monitored.

After 7 days mortality in % is determined. 100% means that all eggs are infertile; 0% means that all eggs are fertile.

In this test for example, the following compounds from the preparation examples showed good activity of 80% at application rate of 20 μg/animal: 1-104

In this test for example, the following compounds from the preparation examples showed good activity of 90% at application rate of 20 μg/animal: 1-27, 1-102

In this test for example, the following compounds from the preparation examples showed good activity of 95% at application rate of 20 μg/animal: 7-5, J-1

In this test for example, the following compounds from the preparation examples showed good activity of 98% at application rate of 20 μg/animal: 1-70, 1-87

In this test for example, the following compounds from the preparation examples showed good activity of 100% at application rate of 20 μg/animal: 1-8, 1-9, 1-10, 1-11, 1-12, 1-16, 1-23, 1-24, 1-25, 1-31, 1-32, 1-34, 1-35, 1-36, 1-37, 1-38, 1-39, 1-47, 1-49, 1-55, 1-56, 1-58, 1-66, 1-67, 1-68, 1-69, 1-72, 1-73, 1-74, 1-75, 1-77, 1-78, 1-79, 1-80, 1-81, 1-86, 1-89, 1-99, 1-101, 1-103, 2-2, 4-2, 5-8, 5-19, 5-21, 5-24, 5-28, 5-29, 5-30, 5-31, 5-32, 5-34, 5-35, 5-36, 5-37, 5-40, 5-41, 5-44, 5-45, 5-46, 5-48, 5-58, 5-59, 5-61, 5-62, 5-78, 5-79, 5-80, 5-81, 5-82, 5-85, 5-86, 5-88, 5-89, 5-90, 5-91, 5-92, 5-93, 5-94, 5-96, 5-100, 5-101, 5-102, 5-103, 5-110, 5-112, 5-117, 5-127, 5-142, 5-144, 5-145, 5-146, 5-147, 5-148, 5-149, 5-150, 5-151, 5-152, 5-153, 5-154, 5-155, 5-157, 5-158, 5-159, 5-160, 5-161, 5-174, 5-175, 5-177, 5-178, 5-179, 5-181, 5-183, 5-187, 5-188, 5-190, 5-192, 5-194, 5-197, 5-198, 5-201, 5-202, 5-203, 5-204, 5-205, 5-206, 5-211, 5-212, 5-213, 5-219, 5-220, 5-221, 6-2, 6-3, 6-4, 6-5, 6-6, 6-7, 9-3, 9-5, 9-6, 10-3, 10-5, 10-6, 10-22, 12-1, A-2, A-3, A-4, F-4, I-5, I-24

After 42 days mortality in % is determined. 100% means that all eggs are infertile; 0% means that all eggs are fertile.

In this test for example, the following compounds from the preparation examples showed good activity of 80% at application rate of 20 μg/animal: 1-7

Biological Test Example 5 Boophilus Microplus (dip)

Solvent: dimethyl sulfoxide

To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 ml solvent, and the concentrate is diluted with water to the desired concentration. Eight to ten adult engorged female Boophilus microplus ticks are placed in perforated plastic beakers and immersed in aqueous compound solution for one minute. Ticks are transferred to a filter paper in a plastic tray. Egg deposition of fertile eggs is monitored after. After 7 days mortality in % is determined 100% means that all the ticks have been killed; 0% means that none of the ticks have been killed. In this test for example, the following compounds from the preparation examples showed good activity of 98% at application rate of 100 ppm: 1-3

Biological Test Example 6 Ctenocephalides Felis—Test (CTECFE)

Solvent: dimethyl sulfoxide

To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 ml solvent, and the concentrate is diluted with cattle blood to the desired concentration. Approximately 20 adult unfed (Ctenocepahlides felis) are placed in flea chambers. The blood chamber, sealed with parafilm on the bottom, are filled with cattle blood supplied with compound solution and placed on top of the flea chamber, so that the fleas are able to suck the blood. The blood chamber is heated to 37° C. whereas the flea chamber is kept at room temperature. After 2 days mortality in % is determined 100% means that all the fleas have been killed; 0% means that none of the fleas have been killed.

In this test for example, the following compounds from the preparation examples showed good activity of 80% at application rate of 100 ppm: 1-3, 1-11, 1-58, 1-75, 1-86, 1-101, 5-46, 5-61, 5-93, 5-100, 5-103, 5-155

In this test for example, the following compounds from the preparation examples showed good activity of 90% at application rate of 100 ppm: 1-9, 1-27, 1-31, 1-32, 1-35, 1-36, 1-47, 1-55, 1-69, 1-79, 2-2, 5-19, 5-21, 5-30, 5-62, 5-67, 5-72, 5-80, 5-82, 5-85, 5-94, 5-96, 5-174, 5-203, 7-5

In this test for example, the following compounds from the preparation examples showed good activity of 95% at application rate of 100 ppm: 1-8, 1-34, 1-49, 1-81, 5-8, 5-24, 5-29, 5-32, 5-65, 5-79, 5-88, 5-89, 5-91, 5-145, 5-147, 5-151, 5-152, 5-175, 5-177, 5-179, 5-181, 5-190, 5-192, 5-198, 5-201, 5-202, 5-221, 9-3, 9-5

In this test for example, the following compounds from the preparation examples showed good activity of 98% at application rate of 100 ppm: 5-139, 5-159

In this test for example, the following compounds from the preparation examples showed good activity of 100% at application rate of 100 ppm: 1-12, 1-38, 1-39, 1-73, 1-77, 1-78, 1-80, 1-89, 5-22, 5-28, 5-31, 5-44, 5-58, 5-77, 5-78, 5-81, 5-86, 5-101, 5-117, 5-127, 5-144, 5-146, 5-148, 5-150, 5-153, 5-154, 5-157, 5-158, 5-160, 5-161, 5-178, 5-194, 5-197, 5-204, 5-205, 5-211, 5-212, 5-213, 5-219, 5-220, 6-2, 6-3, 6-4, 6-5, 6-7, 9-6, 10-3, 10-5, 10-6, 10-22

Biological Test Example 7 Lucilia Cuprina (48 h)

species: Lucilia cuprina 1^(st) instar larvae (age 24 hrs)

solvent: dimethyl sulfoxide

10 mg active compound are dissolve in 0.5 ml Dimethylsulfoxid. Serial dilutions are made to obtain the desired rates. Approximately 20 Lucilia cuprina 1^(st) instar larvae are transferred into a test tube containing 1 cm³ of minced horse meat and 0.5 ml aqueous dilution of test compound. After 48 hrs percentage of larval mortality are recorded. 100% efficacy=all larvae are killed, % efficacy=normally developed larvae after 48 hrs.

In this test for example, the following compounds from the preparation examples showed good activity of 80% at application rate of 100 ppm: 1-27, 1-56, 1-58, 1-72, 5-19, 5-32, 5-80, 5-88, 5-89, 5-91, 5-101, 5-110, 5-117, 5-127, 5-139, 5-187, 5-197, 5-198, 5-201, 6-5, 6-7

In this test for example, the following compounds from the preparation examples showed good activity of 90% at application rate of 100 ppm: 1-35, 1-55, 1-99, 1-103, 5-36, 5-62, 5-81, 5-152, 5-153, 5-179, 5-190, 5-202, 5-204, F-4

In this test for example, the following compounds from the preparation examples showed good activity of 95% at application rate of 100 ppm: 1-12, 5-82, 5-142, 5-146, 5-174, 5-194

In this test for example, the following compounds from the preparation examples showed good activity of 100% at application rate of 100 ppm: 1-3, 1-8, 1-9, 1-11, 1-25, 1-31, 1-35, 1-36, 1-38, 1-39, 1-49, 1-68, 1-69, 1-73, 1-74, 1-75, 1-77, 1-78, 1-79, 1-80, 1-81, 1-89, 2-2, 5-8, 5-22, 5-24, 5-61, 5-72, 5-77, 5-78, 5-85, 5-86, 5-100, 5-144, 5-145, 5-147, 5-148, 5-150, 5-151, 5-154, 5-155, 5-157, 5-158, 5-160, 5-161, 5-211, 5-212, 5-213, 5-219, 5-220, 5-221, 6-2, 6-2, 6-6, 9-3, 9-5, 9-6, 10-3, 10-5, 10-6, A-2, A-3, A-4, I-5, I-24

Biological Test Example 8 Musca Domestica—Test

Solvent: dimethyl sulfoxide

To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 ml solvent, and the concentrate is diluted with water to the desired concentration. Prior to the assay, a piece of kitchen sponge is soaked with a mixture of sugar and compound solution and placed into a container. 10 adults (Musca domestica) are placed into the container and closed with a perforated lid. After 2 days mortality in % is determined 100% means that all the flies have been killed; 0% means that none of the flies have been killed. In this test for example, the following compounds from the preparation examples showed good activity of 80% at application rate of 100 ppm: 1-3, 1-8,1-12, 1-58, 1-73, 1-75, 5-77, 5-88,5-91, 5-103,5-110,5-146, 5-155, 9-6, A-3

In this test for example, the following compounds from the preparation examples showed good activity of 90% at application rate of 100 ppm: 1-11, 1-32, 1-55, 5-78, 5-127, 5-152, 5-153,5-177, 5-198, 5-220

In this test for example, the following compounds from the preparation examples showed good activity of 100% at application rate of 100 ppm: 1-9, 1-39, 1-78, 1-79, 1-80, 1-81, 1-89, 2-2, 5-81, 5-85, 5-89, 5-93, 5-142, 5-148, 5-150, 5-151, 5-154, 5-157, 5-161, 5-175, 5-179, 5-181, 5-192, 5-212, 5-213, 5-211, 5-219, 5-221, 9-3, 10-3, 10-5, 10-6

Preparation Example 1 (Granules)

To a mixture containing 10 parts of the compound of the present invention (No. 1-78), 30 parts of bentonite (montmorillonite), 58 parts of talc and 2 parts of lignin sulfonate was added 25 parts of water, and the mixture was well kneaded and granulated with 10 to 40 meshes by an extruding granulator and dried at 40 to 50° C. to obtain granules.

Preparation Example 2 (Granules)

95 parts of clay mineral granules having particle diameter distribution within the range of 0.2 to 2 mm were put into a rotary mixer, and then wetted evenly by spraying of 5 parts of the compound of the present invention (No. 1-31) together with a liquid diluent under rotating condition and dried at 40 to 50° C. to obtain granules.

Preparation Example 3 (Emulsion)

30 parts of the compound of the present invention (No. 1-31), 55 parts of xylene, 8 parts of polyoxyethylene alkyl phenyl ether and 7 parts of calcium alkylbenzenesulfonate were mixed together to obtain the emulsion.

Preparation Example 4 (Wettable Agent)

15 parts of the compound of the present invention (No. 5-102), 80 parts of a mixture of white carbon (hydrated amorphous silicon oxide fine powder) and powdered clay (1:5), formalin condensate of 2 parts of sodium alkylbenzenesulfonate and 3 parts of sodium alkylnaphthalenesulfonate were mixed together and the mixture was crushed to obtain a wettable agent.

Preparation Example 5 (Wettable Granules)

20 parts of the active compound of the present invention (No. 5-28), 30 parts of lignin sodium sulfonate, 15 parts of bentonite and 35 parts of calcined diatomaceous earth powder were well mixed, and after addition of water, the mixture was then extruded with a screen of 0.3 mm and dried to obtain wettable granules.

Industrial Applicability

The novel pesticidal carboxamides of the present invention have excellent pesticidal activity as shown in the above examples. 

The invention claimed is:
 1. A carboxamide compound of Formula (I-V):

wherein G represents oxygen or sulfur; Q represents hydrogen, C₁₋₁₂ haloalkyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₁₋₁₂ alkoxy)carbonyl or (C₁₋₁₂ hloalkxy)carbonyl; J represents C₁₋₁₂ haloalkyl, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(═O), C₁₋₁₂ haloalkyl-S(═O)₂—, C₃₋₈ halocycloalkyl, —C(J¹) (J²) (J³) or —C(J¹) (J²) (OJ⁴), wherein J¹ and J² each independently represents C₁₋₁₂ haloalkyl, J³ represents a heterocyclic group, and J⁴ represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, alkylsulfonyl, C₁₋₁₂ haloalkylsulfonyl, arylsulfonyl, an aryl group or a heterocyclic group; R1, R2, R4, R5, R7, R8, R9 and R10 each independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, oxide, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(═O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂ alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S (O)—(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂ haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbonyl, (C₃₋₈ halocycloalkoxy)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, (C₃₋₈ halocycloalkyl)-(C₁₋₁₂)alkyl-carbonyl, an aryl group, a heterocyclic group, sulfur pentafluoride, or one of the groups of Formulae (X1-1) to (X1-5):

wherein G is as defined above; X³, X⁴ and X⁵ each independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—,aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyciyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂ alkyl-O—(C₁₋₁₂)alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S(O) —(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂ haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbonyl, (C₃₋₈ halocycloalkoxy)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-carbonyl, aryl-carbonyl, heterocyclyl-carbonyl, aryl-(C₁₋₁₂)alkyl-carbonyl, heterocyclyl-(C₁₋₁₂)alkyl-carbonyl, sulfur pentafluoride, or an aryl group, or X³ and X⁴ optionally forms a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded, or X³ and X⁵ optionally forms a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded, X⁶ represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, C₃₋₈ cycloalkyl, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, an aryl group, a heterocyclic group, aryl-(C₁₋₁₂)alkyl or heterocyclyl-(C₁₋ ₁₂)alkyl, X⁷ represents hydrogen, nitro, cyano, formyl, X⁸-carbonyl or X⁸-oxycarbonyl, and wherein X⁸independently has the same meaning as X⁶ defined above; R12 has the same meaning as X³ defined above; R13 has the same meaning as X⁴ defined above; m represents an integer of 1 to 4; R14 has the same meaning as X³ defined above; and R15 represents hydrogen or has the same meaning as —C(=G)-X⁵, and wherein G and X⁵ are as defined above.
 2. The carboxamide compound according to claim 1, wherein the heterocyclic group represents any one of groups W1 to W9:

wherein Z each independently represents hydrogen, halogen, nitro, cyano, hydroxy, thio, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylthio, C₁₋₆ haloalkylsulfinyl or C₁₋₆ haloalkylsulfonyl; and k represents an integer from 1 to
 4. 3. The carboxamide compound according to claim 1, wherein G represents oxygen or sulfur; Q represents hydrogen, C₁₋₄ haloalkyl, (C₁₋₄ alkyl)carbonyl, (C₁₋₄ haloalkyl)carbonyl, (C₁₋₄ alkoxy)carbonyl or (C₁₋₄ haloalkoxy)carbonyl; J represents C₁₋₄ haloalkyl, C₁₋₄ haloalkyl-O—, C₁₋₄ haloalkyl-S—, C₁₋₄ haloalkyl-S(═O)—, C₁₋₄ haloalkyl-S(═O)₂—, C₃₋₆ halocycloalkyl, —C(J¹) (J²) (J³) or —C(J¹) (J²) (OJ⁴), wherein J¹ and J² each independently represent C₁₋₄ haloalkyl, J³ represents any one of groups W1 to W9:

wherein Z each independently represents hydrogen, halogen, nitro, cyano, hydroxy, thio, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylthio, C₁₋₆ haloalkylsulfinyl or C₁₋₆ haloalkylsulfonyl, and k represents an integer from 1 to 4, J⁴ represents hydrogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ alkylsulfonyl, C₁₋₄ haloalkylsulfonyl, aryl sulfonyl, an aryl group or a heterocyclic group; R1, R2, R4, R5, R7, R8, R9 and R10 each independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, oxide, C₁₋₄ alkyl, C₁₋₄ haloalkyl, aryl-(C₁₋₄)alkyl, heterocyclyl-(C₁₋₄)alkyl, C₁₋₄ alkyl-O—, C₁₋₄ alkyl-NH—, C₁₋₄ alkyl-S—, C₁₋₄ alkyl-S(O)—, C₁₋₄ alkyl-S(O)₂—, C₁₋₄ alkyl-S(O)₂O —, C₁₋₄ haloalkyl-O—, C₁₋₄ haloalkyl-NH—, C₁₋₄ haloalkyl-S—, C₁₋₄ haloalkyl-S(O)—, C₁₋₄ haloalkyl-S(O)₂—, C₁₋₄ haloalkyl-S(═O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₄ alkyl-O—(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—(C₁₋₄)alkyl, C₁₋₄ alkyl-S—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂—(C ₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂O—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-O—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-NH—(C₁₋₄alkyl, C₁₋₄ haloalkyl-S—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)—(C₁₋₄alkyl, C₁₋₄ haloalkyl-S(O)₂—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂O—(C₁₋₄)alkyl, aryl-O—(C₁₋₄)alkyl, aryl-NH—(C₁₋₄)alkyl, aryl-S—(C₁₋₄)alkyl, aryl-S(O)—(C₁₋₄)alkyl, aryl-S(O)₂—(C₁₋₄)alkyl, aryl-S(O)₂O—(C₁₋₄)alkyl, heterocyclyl-O—(C₁₋₄)alkyl, heterocyclyl-NH—(C₁₋₄)alkyl, heterocyclyl-S—(C₁₋₄)alkyl, heterocyclyl-S(O)—(C₁₋₄)alkyl, heterocyclyl-S(O)₂—(C₁₋₄)alkyl, heterocyclyl-S(O)₂O—(C₁₋₄)alkyl, C₃₋₆ cycloalkyl, C₃₋₆ cycloalkyl-(C₁₋₄)alkyl-, C₃₋₆ halocycloalkyl, C₃₋₆ halocycloalkyl-(C₁₋₄)alkyl-, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₂₋₄ haloalkynyl, di(C₁₋₄ alkyl)amino, di(C₁₋₄ haloalkyl)amino, C₃₋₁₂ trialkylsilyl, hydroxyimino(C₁₋₄alkyl, C₁₋₄ alkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂O—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂O—N═(C₁₋₄)alkyl, (C₁₋₄ alkoxy)carbonyl, (C₁₋₄ haloalkoxy)carbonyl, (C₃₋₆ cycloalkoxy)carbonyl, (C₃₋₆ halocycloalkoxy)carbonyl, C₃₋₆ cycloalkyl-(C₁₋₄ alkoxy)carbonyl, C₃₋₆ halocycloalkyl-(C₁₋₄ alkoxy)carbonyl, (C₁₋₄ alkyl)carbonyl, (C₁₋₄ haloalkyl)carbonyl, (C₃₋₆ cycloalkyl)carbonyl, (C₃₋₆ halocycloalkyl)carbonyl, C₃₋₆ cycloalkyl-(C₁₋₄)alkyl-carbonyl, (C₃₋₆ halocycloalkyl)-(C₁₋₄)alkyl-carbonyl, an aryl group, sulfur pentafluoride, or one of the groups of Formulae (X1-1) to (X1-5):

wherein G is as defined above; X³, X⁴ and X⁵ each independently represent hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, C₁₋₄ alkyl, C₁₋₄ haloalkyl, aryl-(C₁₋₄)alkyl, heterocyclyl-(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—, C₁₋₄ alkyl-S—, C₁₋₄ alkyl-S(O)—, C₁₋₄ alkyl-S(O)₂—, C₁₋₄ alkyl-S(O)₂O—, C₁₋₄ haloalkyl-O—, C₁₋₄ haloalkyl-NH—, C₁₋₄ haloalkyl-S—, C₁₋₄ haloalkyl-S(O)—, C₁₋₄ haloalkyl-S(O)₂—, C₁₋₄ haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂-, heterocyclyl-S(O)₂O—, C₁₋₄ alkyl-O—(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—(C₁₋₄)alkyl, C₁₋₄ alkyl-S—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂—(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂O—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-O—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-NH—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O )₂—(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂O—(C₁₋₄)alkyl, aryl-O—(C₁₋₄)alkyl, aryl-NH—(C₁₋₄)alkyl, aryl-S—(C₁₋₄)alkyl, aryl-S(O)—(C₁₋₄)alkyl, aryl-S(O )₂—(C₁₋₄)alkyl, aryl-S(O )₂O—(C₁₋₄)alkyl, heterocyclyl-O—(C₁₋₄)alkyl, heterocyclyl-NH—(C₁₋₄)alkyl, heterocyclyl-S—(C₁₋₄)alkyl, heterocyclyl-S(O)—(C₁₋₄)alkyl, heterocyclyl-S(O)₂—(C₁₋₄)alkyl, heterocyclyl-S(O)₂O—(C₁₋₄)alkyl, C₃₋₆ cycloalkyl, C₃₋₆ cycloalkyl-(C₁₋₄)alkyl-, C₃₋₆ halocycloalkyl, C₃₋₆ halocycloalkyl-(C₁₋₄)alkyl-, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₂₋₄ haloalkynyl, di(C₁₋₄ alkyl)amino, di(C₁₋₄ haloalkyl)amino, C₃₋₁₂ trialkylsilyl, hydroxyimino(C₁₋₄)alkyl, C₁₋₄ alkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ alkyl-S(O)₂O—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-O—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-NH—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂—N═(C₁₋₄)alkyl, C₁₋₄ haloalkyl-S(O)₂O—N═(C₁₋₄) alkyl, (C₁₋₄ haloalkoxy)carbonyl, (C₃₋₆ cycloalkoxy)carbonyl, (C₃₋₆ halocycloalkoxy)carbonyl, C₃₋₆ cycloalkyl-(C₁₋₄alkoxy)carbonyl, C₃₋₆ halocycloalkyl-(C₁₋₄ alkoxy)carbonyl, (C₁₋₄ alkyl)carbonyl, (C₁₋₄ haloalkyl)carbonyl, (C₃₋₆ cycloalkyl)carbonyl, (C₃₋₆ halocycloalkyl)carbonyl, C₃₋₆ cycloalkyl-(C₁₋₄)alkyl-carbonyl, C₃₋₆ halocycloalkyl-(C₁₋₄)alkyl-carbonyl, aryl-carbonyl, heterocyclyl-carbonyl, aryl-(C₁₋₄alkyl-carbonyl, heterocyclyl-(C₁₋₄)alkyl-carbonyl, sulfur pentafluoride, or an aryl group, or X³ and X⁴ optionally form a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded, or X³ and X⁵ optionally form a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded, X⁶ represents hydrogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₆ cycloalkyl, C₂₋₄ alkenyl, C₂₋₄ haloalkenyl, an aryl group, a heterocyclic group, aryl-(C₁₋₄)alkyl or heteroeyelyl-(C₁₋₄)alkyl, and X⁷ represents hydrogen, nitro, cyano, formyl, X⁸-carbonyl or X⁸-oxycarbonyl, and wherein X⁸ independently has the same meaning as X⁶ defined above.
 4. The carboxamide compound according to claim 1, wherein J represents C₁₋₄ perfluoroalkyl, C₁₋₄ monobromoperfluoroalkyl, C₃₋₆ perfluorocycloalkyl, —C (J¹) (J²) (J³) or —C(J¹) (J²) (OJ⁴), J¹ and J² each independently represent C₁₋₄ perfluoroalkyl, J³ represents any one of groups W1 to W9:

wherein Z each independently represents hydrogen, halogen, nitro, cyano, hydroxy, thio, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylthio, C₁₋₆ haloalkylsulfinyl or C₁₋₆ haloalkylsulfonyl, and K represents an integer from 1 to 4; and J⁴ represents C₁₋₄ alkyl, C₁₋₄ haloalkyl or a phenyl group.
 5. The carboxamide compound according to claim 1, wherein G represents oxygen; m represents an integer of 1; and R9, R12 and R13 each represents hydrogen.
 6. A composition comprising at least one compound according to any one of claims 1 to 5, and an extender and/or a surfactant.
 7. An animal parasite-controlling agent comprising at least one compound according to any one of claims 1 to
 5. 8. A carboxamide compound of Formula (I-V):

wherein G represents oxygen or sulfur; Q represents C₁₋₁₂ alkyl; J represents C₁₋₁₂ haloalkyl, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(═O), C₁₋₁₂ haloalkyl-S(═O)₂—, C₃₋₈ halocycloalkyl, —C(J¹) (J²) (J³) or —C(J¹) (J²) (OJ⁴), wherein J¹ and J² each independently represents C₁₋₁₂ haloalkyl, J³ represents a heterocyclic group, and J⁴ represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, alkylsulfonyl, C₁₋₁₂ haloalkylsulfonyl, arylsulfonyl, an aryl group or a heterocyclic group; R1, R2, R4, R5, R7, R8, R9 and R10 each independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, oxide, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(═O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂ alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂ haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbonyl, (C₃₋₈ halocycloalkoxy)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, (C₃₋₈ halocycloalkyl)-(C₁₋₁₂)alkyl-carbonyl, an aryl group, a heterocyclic group, sulfur pentafluoride, or one of the groups of Formulae (X1-1) to (X1-5):

wherein G is as defined above; X³ independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, C₁-₁₂ alkyl, C₁₋₁₂ haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—,aryl-S—, aryl-S—, aryl-S(O)—, aryl-S(O)₂O—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂ alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂ haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbonyl, (C₃₋₈ halocycloalkoxy)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, (C₃₋₈ halocycloalkyl-(C₁₋₁₂alkoxy)carbonyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-carbonyl, aryl-carbonyl, aryl-(C₁₋₁₂)alkyl-carbonyl, heterocyclyl-(C₁₋₁₂)alkyl-carbonyl, or sulfur pentafluoride, or a heterocyclic group, X⁴ independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—, (C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—, (C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂ haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbonyl, (C₃₋₈ halocycloalkoxy)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂ haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-carbonyl, aryl-carbonyl, heterocyclyl-carbonyl, aryl-(C₁₋₁₂)alkyl-carbonyl, heterocyclyl-(C₁₋₁₂)alkyl-carbonyl, or sulfur pentafluoride, an aryl group or a heterocyclic group, X⁵ independently represents hydrogen, cyano, halogen, nitro, hydroxy, mercapto, amino, formyl, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, aryl-(C₁₋₁₂)alkyl, heterocyclyl-(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—, C₁₋₁₂ alkyl-S—, C₁₋₁₂ alkyl-S(O)—, C₁₋₁₂ alkyl-S(O)₂—, C₁₋₁₂ alkyl-S(O)₂O—, C₁₋₁₂ haloalkyl-O—, C₁₋₁₂ haloalkyl-NH—, C₁₋₁₂ haloalkyl-S—, C₁₋₁₂ haloalkyl-S(O)—, C₁₋₁₂ haloalkyl-S(O)₂—, C₁₋₁₂ haloalkyl-S(O)₂O—, aryl-O—, aryl-NH—, aryl-S—, aryl-S(O)—, aryl-S(O)₂—, aryl-S(O)₂O—, heterocyclyl-O—, heterocyclyl-NH—, heterocyclyl-S—, heterocyclyl-S(O)—, heterocyclyl-S(O)₂—, heterocyclyl-S(O)₂O—, C₁₋₁₂ alkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—(C₁₋₁₂)alkyl, aryl-O—(C₁₋₁₂)alkyl, aryl-NH—(C₁₋₁₂)alkyl, aryl-S—(C₁₋₁₂)alkyl, aryl-S(O)—(C₁₋₁₂)alkyl, aryl-S(O)₂—(C₁₋₁₂)alkyl, aryl-S(O)₂O—(C₁₋₁₂)alkyl, heterocyclyl-O—(C₁₋₁₂)alkyl, heterocyclyl-NH—(C₁₋₁₂)alkyl, heterocyclyl-S—(C₁₋₁₂)alkyl, heterocyclyl-S(O)—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂—(C₁₋₁₂)alkyl, heterocyclyl-S(O)₂O—(C₁₋₁₂)alkyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-, C₃₋₈ halocycloalkyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-, C₂₋₁₂ alkenyl, C₂₋₁₂ haloalkenyl, C₂₋₁₂ alkynyl, C₂₋₁₂ haloalkynyl, di(C₁₋₁₂ alkyl)amino, di(C₁₋₁₂haloalkyl)amino, C₃₋₃₆ trialkylsilyl, hydroxyimino(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-O—N—(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ alkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-O—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-NH—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂—N═(C₁₋₁₂)alkyl, C₁₋₁₂ haloalkyl-S(O)₂O—N═(C₁₋₁₂)alkyl, (C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ haloalkoxy)carbonyl, (C₃₋₈ cycloalkoxy)carbonyl, (C₃₋₈ halocycloalkoxy)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂ alkoxy)carbonyl, (C₁₋₁₂ alkyl)carbonyl, (C₁₋₁₂haloalkyl)carbonyl, (C₃₋₈ cycloalkyl)carbonyl, (C₃₋₈ halocycloalkyl)carbonyl, C₃₋₈ cycloalkyl-(C₁₋₁₂)alkyl-carbonyl, C₃₋₈ halocycloalkyl-(C₁₋₁₂)alkyl-carbonyl, aryl-carbonyl, aryl-(C₁₋₁₂)alkyl-carbonyl, heterocyclyl-(C₁₋₁₂)alkyl-carbonyl, or sulfur pentafluoride, an aryl group, or X³ and X⁴ optionally forms a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded, or X³ and X⁵ optionally forms a heterocycle together with the nitrogen atom, carbon atom, oxygen atom or sulfur atom to which they are bonded, X⁶ represents hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ haloalkyl, C₃₋₈ cycloalkyl, C_(2-12 alkenyl, C) ₂₋₁₂ haloalkenyl, an aryl group, a heterocyclic group, aryl-(C₁₋₁₂)alkyl or heterocyclyl-(C₁₋₁₂)alkyl, X⁷ represents hydrogen, nitro, cyano, formyl, X⁸-carbonyl or X⁸-oxycarbonyl, and wherein X⁸ independently has the same meaning as X⁶ defined above; R12 has the same meaning as X³ defined above; R13 has the same meaning as X⁴ defined above; m represents an integer of 1 to 4; R14 has the same meaning as X³ defined above; and R15 represents —C(═G)—X⁵, and wherein G and X⁵ are as defined above. 